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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604711Generated: October 31, 2026

Benzo(B)Thiophene → 1-Benzothien-2-yl(5-bromo-2-chlorophenyl)methanol

https://huagongshe.com/reaction/604711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo(B)ThiopheneHCID 7221—
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Bromo-2-chlorobenzaldehydeHCID 10608925—
SolventTetrahydrofuranHCID 8028—
Product1-Benzothien-2-yl(5-bromo-2-chlorophenyl)methanolHCID 2310338371%

Reaction Steps

1.6 M n-butylithium hexane solution (26.9 mL) was added to a mixture of benzo[b]thiophene (5.8 g, 0.043 mol) and tetrahydrofuran (58 mL) at −78° C. over 20 minutes. After stirred for 0.5 hours, the mixture was added with a tetrahydrofuran (50 mL) solution of 5-bromo-2-chlorobenzaldehyde (9.0 g, 0.041 mol) and stirred for further five minutes. The reaction mixture was warmed to room temperature. After the reaction mixture was added with a saturated ammonium chloride aqueous solution and extracted with ethyl acetate, the organic phase was washed with brine and then dried with anhydrous magnesium sulfate. After the desiccant was filtered off, the residue obtained by evaporating the solvent under reduced pressure was purified by silica gel column chromatography (hexane:ethyl acetate=10:1) to obtain pale yellow oily (1-benzothien-2-yl)(5-bromo-2-chlorophenyl)methanol (10.3 g, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910619B2
Source datasetuspto-grants-2011_03
ORD IDord-4cbfe4ff0d7d42128f5706414c81cdb5
Source noteuspto-grants-2011_03