| Identification | Back Directory | [Name]
4-Aminotetrahydro-2H-thiopyran 1,1-dioxide | [CAS]
210240-20-3 | [Synonyms]
NSC106913
1,1-dioxothian-4-amine
1,1-dioxo-4-thianamine hydrochloride
1,1-dioxothian-4-amine hydrochloride
1,1-Dioxo-tetrahydrothiopyran-4-aMine
4-Aminotetrahydrothiopyran 1,1-Dioxide
(1,1-diketothian-4-yl)amine hydrochloride
4-Aminotetrahydro-2H-thiopyran 1,1-dioxide
Tetrahydro-2H-thiopyran-4-amine 1,1-dioxide
2H-Thiopyran-4-aMine, tetrahydro-, 1,1-dioxide
2H-Thiopyran-4-amine,tetrahydro-,1,1-dioxide(9CI)
Thiopyran, 4-aminotetrahydro-, 1,1-dioxide, hydrochloride
(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)amine(SALTDATA: HCl) | [Molecular Formula]
C5H11NO2S | [MDL Number]
MFCD09540491 | [MOL File]
210240-20-3.mol | [Molecular Weight]
149.21 |
| Chemical Properties | Back Directory | [Boiling point ]
339.7±35.0 °C(Predicted) | [density ]
1.237 | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [pka]
8.32±0.20(Predicted) | [Appearance]
Off-white to light yellow Solid |
| Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 4-aminotetrahydro-2H-thiopyran 1,1-dioxide from the compound (CAS:99586-63-7): to a stirred methanolic solution of compound 4.3 (0.14 g, 0.85 mmol) was added Raney Ni catalyst and the resulting mixture was stirred and reacted for 3 hours at room temperature in hydrogen atmosphere. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction mixture was filtered and the methanolic filtrate was concentrated under reduced pressure to afford the target product 4-aminotetrahydro-2H-thiopyran 1,1-dioxide (Compound 4.4, 0.10 g, 78% yield). | [References]
[1] Patent: US2009/82423, 2009, A1. Location in patent: Page/Page column 24
[2] Journal of the American Chemical Society, 1955, vol. 77, p. 3866,3867 |
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