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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066817Generated: November 2, 2026

Dichloromethane → HCID 21196095, compound

https://huagongshe.com/reaction/1066817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant4-Bromo-2-(bromomethyl)-1-fluorobenzeneHCID 13553295—
ReactantCarbamic acid, (4-hydroxy-2,2-dimethylbutyl)-, 1,1-dimethylethyl esterHCID 21196111—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21196095HCID 2119609574.2%

Reaction Conditions

Temperature-45 °C

Reaction Steps

A stirred solution of 4-(t-butoxycarbonylamino)-3,3-dimethylbutan-1-ol (1.0 g, 4.60 mmol) in tetrahydrofuran (33 ml) at −45° C. was treated with potassium t-butoxide (1 M in tetrahydrofuran, 5.06 ml, 5.06 mmol). The anion was stirred for 30 minutes at −45° C., then cooled to −78° C. and treated with a tetrahydrofuran solution of 2-fluoro-5-bromobenzyl bromide (1.23 g, 4.60 mmol). The resulting yellow mixture was slowly warmed to 0° C. and stirred for about four hours. The cloudy reaction mixture was diluted wtih methylene chloride (100 ml) and washed with 1 M potassium carbonate. The organic fraction was dried over sodium sulfate, filtered, and the solvents were removed in vacuo. The residue was further purified by preparative high performance liquid chromatography to yield 1.38 grams (74%) of the title intermediate as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245761B1
Source datasetuspto-grants-2001_06
ORD IDord-263070a68c5046078afcb7451df50e5a
Source noteuspto-grants-2001_06