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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721230Generated: November 2, 2026

tert-Butanol → Tert-butyl 4-(bromomethyl)benzoate

https://huagongshe.com/reaction/1721230

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant1,1-Dimethylethyl 4-methylbenzoateHCID 11629749—
SolventCarbon TetrachlorideHCID 5943—
ProductTert-butyl 4-(bromomethyl)benzoateHCID 1141457840%

Reaction Steps

N-Bromosuccinimide (NBS) (35.8 g, 0.20 mol) was added in several portions to a solution of 1,1-dimethylethyl 4-methylbenzoate (prepared by the reaction of the respective acid chloride with t-butanol.) (38.0 g, 0.20 mol) and benzoyl peroxide (0.36 g, 1.5 mmol) in carbon tetrachloride (1200 mL) at vigorous reflux. Another portion of benzoyl peroxide (0.36 g, 1.5 mmol) was added just before the final addition of NBS. After the foaming subsided, the reaction mixture was cooled to room temperature, washed with water (2×60 mL) and dried over magnesium sulfate. Filtration and concentration provided an oil that was purified by HPLC on silica gel eluting with a mixture of hexanes and ethyl acetate to give 1,1-dimethylethyl 4-bromomethylbenzoate (21.4 g) in 40% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05508437
Source datasetuspto-grants-1996_04
ORD IDord-58e74c38dbb944c8aa833bef0ae515b3
Source noteuspto-grants-1996_04