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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709405Generated: October 27, 2026

Triethylamine → (trans)-2-(4-Bromophenyl)cyclopropanecarbonyl azide

https://huagongshe.com/reaction/709405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium AzideHCID 33557—
Reactantrac-(1R,2R)-2-(4-bromophenyl)cyclopropane-1-carboxylic acidHCID 12586658—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product(trans)-2-(4-Bromophenyl)cyclopropanecarbonyl azideHCID 8669119091.1%

Reaction Steps

Ethyl chloroformate (1.9 mL) was added to a solution of (trans)-2-(4-bromophenyl) cyclopropanecarboxylic acid (Intermediate J, 4 g, 0.0165 mol) and Et3N (2.51 mL, 0.0199 mol) in acetone (60 mL) at −20° C., stirred at same temperature for 1 h, then a solution of NaN3 (1.3 g, 0.0199 mol) in water (5 mL), was added and stirred for 30 mins at rt. After completion of reaction, checked by TLC, the solvent was evaporated and crude residue was dissolved in ethyl acetate (100 mL), washed with water (40 mL), dried over anhydrous Na2SO4, filtered and evaporated to get (trans)-2-(4-bromophenyl)cyclopropanecarbonyl azide (4 g). The crude residue is carried to next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181198B2
Source datasetuspto-grants-2015_11
ORD IDord-d3dfa92e9d264ce88ce59f862d867569
Source noteuspto-grants-2015_11