ChemicalBook CAS DataBase List 7-bromochroman-4-one

7-bromochroman-4-one synthesis

11synthesis methods

Product Name:7-bromochroman-4-one
CAS Number:18442-22-3
Molecular formula:C9H7BrO2
Molecular Weight:227.05

7-Bromochroman-4-one was synthesized by hydrogenation addition of 7-Bromo-benzopyrone catalyzed by Wilkinson's catalyst Rhodium( Ⅰ) tris( triphenylphosphine) chloride[Rh( PPh3)3Cl]. The structure was confirmed by1 H NMR and MS. The optimum reaction conditions for synthesizing 7-Bromochroman-4-one were as follows: 5 0. 329 mol,ethanol as the solvent,c( 5) =0. 4 mol·L- 1,4% mol Rh( PPh3)3Cl as the catalyst,under 0. 3 MPa of hydrogen pressure,at 70℃ for 20 h,the yield was 79. 8%.

18386-03-3 Synthesis

18386-03-3
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$148.00/100mg

18442-22-3
135 suppliers
$12.00/250mg

Yield:18442-22-3 85%

Reaction Conditions:

with acid activated montmorillonite K-10 in toluene; for 0.5 h;Reflux;Inert atmosphere;

Steps:

General experimental procedure for the synthesis of chroman-4-one (4a-4p)

General procedure: A mixture of 3-aryloxypropionic acid 3a-3o (1.0 mmol) and freshly prepared AA.Mont.K-10 (300% by weight) in toluene (2 mL) was heated to reflux under inert atmosphere for the specified time (30-45 minutes). After reaction completion, reaction mixture is cooled and added CH₂Cl₂ (10-15 mL). Filtered the AA.Mont.K-10 and washed twice with CH₂Cl₂. The organic filtrate is concentrated and the crude mass is extracted with hexane (10-15 mL) to afford pure chromanones 4a-4p.

References:

Begum, Ayisha F.;Balasubramanian, Kalpattu K.;Shanmugasundaram, Bhagavathy [Tetrahedron Letters,2021,vol. 82,art. no. 153372] Location in patent:supporting information

168759-60-2
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18442-22-3
135 suppliers
$12.00/250mg

References

491-37-2
290 suppliers
$6.00/1g

18442-22-3
135 suppliers
$12.00/250mg

References

91763-35-8
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18442-22-3
135 suppliers
$12.00/250mg

References

Benzene, 1-bromo-3-[(3-chloro-2-propyn-1-yl)oxy]-

890840-78-5
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18442-22-3
135 suppliers
$12.00/250mg

References

7-bromochroman-4-one Related Search:

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