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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475625Generated: November 2, 2026

Benzylamine → tert-Butyl 1-[3-(benzylamino)-4-chlorobenzyl]cyclopropanecarboxylate

https://huagongshe.com/reaction/1475625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
Reactanttert-Butyl 1-(3-bromo-4-chlorobenzyl)cyclopropanecarboxylateHCID 67958496—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Producttert-Butyl 1-[3-(benzylamino)-4-chlorobenzyl]cyclopropanecarboxylateHCID 68006927—

Reaction Conditions

Temperature110 °C

Reaction Steps

Under argon, 95.0 g (274.8 mmol) of tert-butyl 1-(3-bromo-4-chlorobenzyl)cyclopropanecarboxylate, 36.0 ml (330.0 mmol) of benzylamine, 12.58 g (13.7 mmol) of tris(dibenzylideneacetone)dipalladium, 31.69 g (329.8 mmol) of sodium tert-butoxide and 6.85 g (5.29 mmol) of (+/−)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl were added in succession to 633 ml of dry toluene. The reaction mixture was stirred at 110° C. for 3.0 h and then at RT overnight. The reaction mixture was then filtered off with suction through kieselguhr, and the residue was washed thoroughly with toluene and ethyl acetate. The combined filtrates were concentrated under reduced pressure. The crude product was purified by chromatography on silica gel (mobile phase petroleum ether/ethyl acetate 10:1). This gave 50.0 g of the title compound (48.9% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018258B2
Source datasetuspto-grants-2015_04
ORD IDord-68528a99bd5547c29d50c926df13303c
Source noteuspto-grants-2015_04