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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746094Generated: November 1, 2026

Potassium Carbonate → Tert-butyl(trans)-2-(4-(3-bromobenzyloxy)phenyl)cyclopropylcarbamate

https://huagongshe.com/reaction/1746094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromobenzyl bromideHCID 69979—
Reactanttert-Butyl N-[(1R,2S)-rel-2-(4-hydroxyphenyl)cyclopropyl]carbamateHCID 86672576—
SolventDimethylformamideHCID 6228—
ProductTert-butyl(trans)-2-(4-(3-bromobenzyloxy)phenyl)cyclopropylcarbamateHCID 8668087362.2%

Reaction Steps

To a solution of tert-butyl-(trans)-2-(4-hydroxyphenyl)cyclopropylcarbamate (Intermediate N, 5 g, 20.0 mmol), K2CO3 (6.8 g, 50.0 mmol) in dry DMF (10 vols) was added 3-Bromo benzyl bromide (5 g, 20.0 mmol) and stirred at RT for 16 h. After completion, the reaction mixture was poured into ice water (150 mL) and extracted with EtOAc (2×75 mL). The combined extracts were washed with water (100 mL), brine (100 mL), dried over anhydrous Na2SO4, filtered and evaporated. The crude residue was purified by flash chromatography to give (tert-butyl(trans)-2-(4-(3-bromobenzyloxy)phenyl)cyclopropylcarbamate (5.2 g, 62%) as a white solid. The crude was carried to next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09149447B2
Source datasetuspto-grants-2015_10
ORD IDord-8e6c61a8e85c4ffdbc05061fc600898c
Source noteuspto-grants-2015_10