HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 609545Generated: October 30, 2026
tert-Butanol → N-1-Boc-Amino-3-cyclopentene
https://huagongshe.com/reaction/609545
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 3-Cyclopentene-1-carboxylic acid | HCID 853756 | — |
| Product | N-1-Boc-Amino-3-cyclopentene | HCID 2756764 | — |
Reaction Steps
To a solution of 3-cyclopentene-1-carboxylic acid (J.-P. Depres and A. E. Greene, J. Org. Chem. 1984, 49:928-931; 29.71 g, 0.261 mole), triethylamine (36.4 mL) in t-butanol (1 L) was added diphenylphosphoryl azide, Aldrich, 97%, 74.0 g, 0.261 mmole). The solution was maintained at 60--C. for 4 hours. Cuprous chloride (1.3 g) was added and stirring continued at ambient temperature for 18 hours. Volatiles were evaporated and the residue was dissolved in methylene chloride (1250 mL) and washed with 10 % aqueous sodium carbonate (2×250 mL) and dried (magnesium sulfate). Volatiles were evaporated and the residue was chromatographed on a silica gel column. Title compound was eluted with chloroform as white crystals, from hexanes (22.63 g, 47%), m.p. 68-70° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05998398 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-7d52b3919c5145259226aa4612df7ffd |
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| Source note | uspto-grants-1999_12 |
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