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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427003Generated: October 30, 2026

[2-(t-Butoxycarbonylaminomethyl)-1,4-cyclohexadienyl]acetic acid → [2-(N-t-Butoxycarbonylaminomethyl)-1-cyclohexen-1-yl]acetic acid

https://huagongshe.com/reaction/427003

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[2-(t-Butoxycarbonylaminomethyl)-1,4-cyclohexadienyl]acetic acidHCID 15918136—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAmmonium HydroxideHCID 14923—
Product[2-(N-t-Butoxycarbonylaminomethyl)-1-cyclohexen-1-yl]acetic acidHCID 15918137—

Reaction Steps

A solution of α-[2-(t-butoxycarbonylaminomethyl)-1,4-cyclohexadienyl]-acetic acid (1.33 g., 5 mmoles) in 3% ammonium hydroxide (10 ml.) was hydrogenated at 40 psi with palladium on charcoal (10%, 0.2 g.). A theoretical amount of hydrogen was taken up in 3 hours. The catalyst was removed and the filtrate was acidified to pH 2 with dil. HCl and extracted with ethyl acetate (2×50 ml.). The combined extracts were washed with water (20 ml.), dried with Na2SO4 and evaporated under reduced pressure to afford an oil (1.34 g.) which solidified on standing for several days. Recrystallization from n-hexane - ethyl acetate gave 1.2 g. title product as colorless prisms melting at 118°-119° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04172199
Source datasetuspto-grants-1979_10
ORD IDord-93b72fad863a464bbe97303d89077afc
Source noteuspto-grants-1979_10