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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561991Generated: November 2, 2026

(R)-[4-(2-benzyloxy-1-benzyloxymethyl-ethoxy)-phenyl]-tert-butoxycarbonylamino-acetic acid → (R)-tert-butoxycarbonylamino-[4-(2-hydroxy-1-hydroxymethyl-ethoxy)-phenyl]-acetic acid

https://huagongshe.com/reaction/561991

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-[4-(2-benzyloxy-1-benzyloxymethyl-ethoxy)-phenyl]-tert-butoxycarbonylamino-acetic acidHCID 67001437—
SolventMethanolHCID 887—
Product(R)-tert-butoxycarbonylamino-[4-(2-hydroxy-1-hydroxymethyl-ethoxy)-phenyl]-acetic acidHCID 67001303—

Reaction Steps

A hydrogenation vessel containing a solution of (R)-[4-(2-benzyloxy-1-benzyloxymethyl-ethoxy)-phenyl]-tert-butoxycarbonylamino-acetic acid (3.86 g, 7.4 mmol) in methanol (30 mL) was purged with nitrogen and 10% palladium on carbon (300 mg) added. The atmosphere above the methanol solution was exchanged for hydrogen and the reaction mixture stirred vigorously for 30 minutes at ambient temperature. The reaction mixture was filtered through a pad of celite and concentrated in vacuo to give (R)-tert-butoxycarbonylamino-[4-(2-hydroxy-1-hydroxymethyl-ethoxy)-phenyl]-acetic acid which was used without additional purification (2.43 g, 96%). HR-MS: calcd for C30H28FlN4O5 [M+H+] 671.1161. Found 671.1158.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063085B2
Source datasetuspto-grants-2011_11
ORD IDord-923cc0fcb87d4b55ba21381faad02c6f
Source noteuspto-grants-2011_11