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 2h. 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 | US05925624 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-f79d2b6ba67a4756968baf3fe0b07dc3 |
| Source note | uspto-grants-1999_07 |