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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050983Generated: October 27, 2026

Boron tribromide → (4,4-Dimethyl-6-thiochromanoyloxy)benzoic acid

https://huagongshe.com/reaction/2050983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantBenzyl 4-(4,4-dimethyl-6-thiochromanoyloxy)benzoateHCID 19834230—
SolventDichloromethaneHCID 6344—
Product(4,4-Dimethyl-6-thiochromanoyloxy)benzoic acidHCID 19834232—

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a stirred solution of 580 mg (1.34) of benzyl 4-(4,4-dimethyl-6-thiochromanoyloxy)benzoate in 12 ml of methylene chloride at -10° C. under nitrogen was added slowly 1.24 ml of a 1.0M (1.24 mmol) solution of boron tribromide in methylene chloride. The reaction mixture was stirred at -10° C. for a further 2 h and then was quenched by the addition of ice. The organic layer was separated and the aqueous layer extracted with 2×25 ml methylene chloride. The organic extracts were combined and then washed with water and dried (MgSO4). The solution was then filtered and the solvent removed in-vacuo. The resultant residue was purified by flash chromatography (silica; 20% ethyl acetate in hexane followed by 100% ethyl acetate) and then recrystallization from a mixture of ethyl acetate and ethanol to give the title compound as a white solid. PMR (CDCl3): δ1.39 (6H, s), 2.10 (2H, m), 3.10 (2 H, m), 7.21 (1H, d, J~8.4 Hz), 7.28 (2H, d, J~8.7 Hz), 7.82 (1H, dd, J~8.4, 2.1 Hz), 8.14 (2H, d, J~8.7 Hz), 8.16 (1H, d, J~2.1 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05015658
Source datasetuspto-grants-1991_05
ORD IDord-4669175e24524016be3f6ed8d70b3180
Source noteuspto-grants-1991_05