| Identification | Back Directory | [Name]
TETRAHYDRO-2-(2-PROPYNYLOXY)-2H-PYRAN | [CAS]
6089-04-9 | [Synonyms]
2-Propargyloxane
pent-4-ynoic acid
TIMTEC-BB SBB008982
2-Propynyl 2-pyranyl ether
Tetrahydropyran-2-yloxypropyne
2-(Propargyloxy)tetrahydropyran
2-(2-PROPYNYLOXY)TETRAHYDROPYRAN
Tetrahydropyranyl propargyl ether
Tetrahydro-2-(2-propynyloxy)pyran
3-(2'-Tetrahydropyranyloxy)propyne
3-(Tetrahydro-2-pyranyloxy)propyne
Propargyl 2-tetrahydropyranyl ether
3-(tetrahydropyran-2'-yloxy)propyne
2-(2-Propynyloxy)tetrahydro-2H-pyran
2-(prop-2-ynyloxy)tetrahydro-2H-pyran
TETRAHYDRO-2-(2-PROPYNYLOXY)-2H-PYRAN
1-(2'-Tetrahydropyranyloxy)-2-propyne
2-(Prop-2-yn-1-yloxy)tetrahydro-2H-pyran
2-(2-Propynyloxy)tetrahydro-2H-pyran,98%
Tetrahydro-2-(2-propyn-1-yloxy)-2H-pyran
Tetrahydro-2-(2-propynyloxy)-2H-pyran 98%
Propargyl(tetrahydro-2H-pyran-2-yl) ether
2-Propynyl tetrahydro-2H-pyran-2-yl ether
Propargyl alcohol tetrahydropyranyl ether
2H-Pyran, tetrahydro-2-(2-propyn-1-yloxy)-
TETRAHYDRO-2-(2-PROPYNYLOXY)-2H-PYRAN, 9 8%
PROPARGYL ALCOHOL TETRAHYDRO-2H-PYRAN ETHER
(Tetrahydro-2H-pyran-2-yl)(2-propynyl) ether
2-(2-Propynyloxy)tetrahydro-2H-pyran, 98% 5GR
1-(3,4,5,6-Tetrahydro-2H-pyran-2-yloxy)-2-propyne | [EINECS(EC#)]
228-028-0 | [Molecular Formula]
C8H12O2 | [MDL Number]
MFCD00006604 | [MOL File]
6089-04-9.mol | [Molecular Weight]
140.18 |
| Chemical Properties | Back Directory | [Appearance]
Clear colorless to light yellow liquid | [Boiling point ]
63-65 °C9 mm Hg(lit.)
| [density ]
0.997 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.458(lit.)
| [Fp ]
139 °F
| [storage temp. ]
2-8°C | [form ]
Liquid | [color ]
Clear colorless to light yellow | [Specific Gravity]
0.997 | [InChI]
InChI=1S/C8H12O2/c1-2-6-9-8-5-3-4-7-10-8/h1,8H,3-7H2 | [InChIKey]
RNRIMDSCBRDPLC-UHFFFAOYSA-N | [SMILES]
C1(OCC#C)OCCCC1 | [CAS DataBase Reference]
6089-04-9 |
| Hazard Information | Back Directory | [Chemical Properties]
Clear colorless to light yellow liquid | [Uses]
Tetrahydro-2-(2-propynyloxy)-2H-pyran was used in preparation of 1,3-dienyl acetal. | [Synthesis Reference(s)]
Chemistry Letters, 6, p. 817, 1977
Organic Syntheses, Coll. Vol. 7, p. 334, 1990
Synthetic Communications, 19, p. 901, 1989 DOI: 10.1080/00397918908051010 | [General Description]
The anion formed by metalation at the acetylenic carbon reacts with a variety of electrophiles. | [Synthesis]
General procedure for the synthesis of O-THP propargyl alcohol (Compound 18) from 3,4-dihydro-2H-pyran and 2-propyn-1-ol: Compound 18 was prepared according to literature procedure. To a solution of propargyl alcohol 17 (2.6 mL, 44.6 mmol) and p-toluenesulfonic acid monohydrate (0.09 g, 0.5 mmol) in dichloromethane (45 mL) was added dropwise 3,4-dihydro-2H-pyran (4.3 mL, 46.8 mmol) at 0 °C. The reaction mixture was stirred at 0 °C for 5 min before slowly warming up to room temperature and continued stirring for 1 h. The reaction mixture was then purified with aqueous solution of saturated 2H-pyran (4.3 mL). Subsequently, the reaction mixture was washed with saturated sodium bicarbonate solution (30 mL) and the aqueous layer was extracted with dichloromethane (45 mL). The organic layers were combined, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give compound 18 (6.1 g, 97.2% yield) as a yellow oil. Thin layer chromatography (TLC) Rf = 0.30 (hexane/ether, 95:5). 1H NMR (400 MHz, CDCl3): δ = 1.50-1.67 (m, 4H), 1.70-1.89 (m, 2H), 2.41 (t, J = 2.4 Hz, 1H), 3.52-3.57 (m, 1H), 3.82-3.87 (m , 1H), 4.27 (ddd, J = 2.4 Hz, 11.3 Hz, 15.8 Hz, 2H), 4.83 (t, J = 3.4 Hz, 1H). 13C NMR (100 MHz, CDCl3): δ = 19.0, 25.3, 30.2, 53.9, 61.9, 74.0, 79.7, 96.8. mass spectra (MS-CI): m/z calculated values. ): m/z calculated value C8H12O2 [M + H]+, 141; measured value: 141. The synthesis of this compound has been reported in the literature. | [References]
[1] Synlett, 2003, # 14, p. 2163 - 2166
[2] Tetrahedron, 2010, vol. 66, # 25, p. 4573 - 4576
[3] Synthesis, 2005, # 19, p. 3293 - 3296
[4] Journal of the Chinese Chemical Society, 2007, vol. 54, # 2, p. 525 - 532
[5] Journal of Organic Chemistry, 2009, vol. 74, # 4, p. 1531 - 1540 |
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