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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221138Generated: October 31, 2026

tert-Butanol → tert-Butyl 5-bromo-2-chlorobenzoate

https://huagongshe.com/reaction/221138

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
Reactant5-Bromo-2-chlorobenzoic acidHCID 33127—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 5-bromo-2-chlorobenzoateHCID 2229184686.1%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 5-bromo-2-chlorobenzoic acid (11.75 g) in N,N-dimethylformamide (50 ml) was added 1,1′-carbonyldiimidazole (8.10 g), and the mixture was stirred under heating at 40° C. for one hour. Thereto were added t-butanol (7.40 g) and 1,8-diazabicyclo[5.4.0]undec-7-ene (7.60 g), and the mixture was further stirred under heating at 40° C. overnight. The mixture was diluted with diethyl ether, and washed successively with water (3 times), 2% aqueous hydrochloric acid solution (twice), a saturated aqueous sodium hydrogen carbonate solution and brine. The mixture was dried over magnesium sulfate, and the solvent was evaporated under reduced pressure to give t-butyl 5-bromo-2-chlorobenzoate (12.53 g) as pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202984B2
Source datasetuspto-grants-2012_06
ORD IDord-93276b101afb4b2e8ab7b07031a946ed
Source noteuspto-grants-2012_06