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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420303Generated: October 26, 2026

Formic Acid → (1S,3S)-3-[(tert-Butoxycarbonyl)amino]cyclopentyl formate

https://huagongshe.com/reaction/1420303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant1,1-Dimethylethyl N-((1S,3R)-3-hydroxycyclopentyl)carbamateHCID 21637081—
Product(1S,3S)-3-[(tert-Butoxycarbonyl)amino]cyclopentyl formateHCID 8675402350.1%

Reaction Steps

Diethyl azodicarboxylate (0.164 ml, 1.23 mmol) was added dropwise to a stirred solution of (1S-cis)-(3-hydroxycyclopentyl)carbamic acid 1,1-dimethylethyl ester (0.124 g, 0.61 mmol), triphenylphosphine (0.323 g, 1.23 mmol) and formic acid (0.046 ml, 1.23 mmol) and the solution was stirred at room temperature for 2 h The solution was then concentrated and purified by column chromatography on flash silica eluting with 10-30% ethyl acetate in cyclohexane to give the title compound (0.07 g) as white needles from diisopropyl ether m p.84°-85° C., [α]D -12.7° (CHCl3 c=0.55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05889178
Source datasetuspto-grants-1999_03
ORD IDord-a80029c921c94de0bd02af561661f190
Source noteuspto-grants-1999_03