Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365013Generated: October 30, 2026

Sodium Hydroxide → 1-(Tert-butoxycarbonylamino)-2-(difluoromethyl)cyclopropanecarboxylic acid

https://huagongshe.com/reaction/1365013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 1-((benzyloxycarbonyl)(tert-butoxycarbonyl)amino)-2-(difluoromethyl)cyclopropanecarboxylateHCID 57945033—
ReactantMethyl 1-(tert-butoxycarbonylamino)-2-(difluoromethyl)cyclopropanecarboxylateHCID 66752484—
SolventMethanolHCID 887—
Product1-(Tert-butoxycarbonylamino)-2-(difluoromethyl)cyclopropanecarboxylic acidHCID 57945043151.3%

Reaction Steps

A mixture of methyl 1-((benzyloxycarbonyl)(tert-butoxycarbonyl)amino)-2-(difluoromethyl)cyclopropanecarboxylate (1.05 g, 2.63 mmol), methyl 1-(tert-butoxycarbonylamino)-2-(difluoromethyl)cyclopropanecarboxylate (1.43 g, 5.39 mmol) in MeOH (20 mL) and sodium hydroxide (10 mL, 40.0 mmol) was stirred at rt for 18 h. The reaction mixture was concentrated and adjusted to pH=4 using 1N HCl. A white solid precipitated from the solution and was collected by filteration. The filter cake was washed with water to yield 1.2 g of the crude product as a white solid. Crystallization from hexane/EtOAc gave 1.0 g (50%) of 1-(tert-butoxycarbonylamino)-2-(difluoromethyl)cyclopropanecarboxylic acid as a white solid. This intermediate was isolated as a single diastereoisomer wherein the CF2H substituent is syn to the carboxyl group.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888464B2
Source datasetuspto-grants-2011_02
ORD IDord-0d036ed8ecab4a14a48ec2a4d0714625
Source noteuspto-grants-2011_02