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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626410Generated: October 30, 2026

tert-Butyl 1-[3-(benzylamino)-4-fluorobenzyl]cyclopropanecarboxylate → tert-Butyl 1-(3-amino-4-fluorobenzyl)cyclopropanecarboxylate

https://huagongshe.com/reaction/626410

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 1-[3-(benzylamino)-4-fluorobenzyl]cyclopropanecarboxylateHCID 58136659—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
Producttert-Butyl 1-(3-amino-4-fluorobenzyl)cyclopropanecarboxylateHCID 58136688—

Reaction Steps

145.0 g (407.9 mmol) of tert-butyl 1-[3-(benzylamino)-4-fluorobenzyl]cyclopropanecarboxylate were dissolved in 1450 ml of ethanol, and 9.67 g of palladium hydroxide (20% on carbon) were added. The suspension was stirred at RT under a hydrogen atmosphere at standard pressure for 18 h. The reaction mixture was then filtered off with suction through kieselguhr, and the filtrate was concentrated. After drying under high vacuum, 500 ml of pentane were added to the residue, resulting in the precipitation of the product. The suspension was stirred in an ice bath for 1 h. The solid was then filtered off with suction, washed twice with pentane and dried under high vacuum. 88.5 g (73.6% of theory) of the title compound were thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309198B2
Source datasetuspto-grants-2016_04
ORD IDord-e9932671c9f54a9aa732e04f2d3b85a2
Source noteuspto-grants-2016_04