HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → (1S,3S)-3-[(tert-Butoxycarbonyl)amino]cyclopentyl formate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 1,1-Dimethylethyl N-((1S,3R)-3-hydroxycyclopentyl)carbamate | HCID 21637081 | — |
| Product | (1S,3S)-3-[(tert-Butoxycarbonyl)amino]cyclopentyl formate | HCID 86754023 | 50.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05889178 |
| Source dataset | uspto-grants-1999_03 |
| ORD ID | ord-a80029c921c94de0bd02af561661f190 |
| Source note | uspto-grants-1999_03 |