HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374415Generated: November 1, 2026
Water → tert-butyl (4R)-4-{[(benzyloxy)carbonyl]amino}pentanoate
https://huagongshe.com/reaction/1374415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | HCID 69349527 | HCID 69349527 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | tert-butyl (4R)-4-{[(benzyloxy)carbonyl]amino}pentanoate | HCID 11109586 | 98% |
Reaction Steps
To a solution of tert-butyl(4S)-4-{[(benzyloxy)carbonyl]amino}-5-bromopentanoate (4.5 g, 11.7 mmol) and tributyltin hydride (6.3 ml, 23.4 mmol) in toluene (45 ml) was added 2,2′-azobisisobutyronitrile (0.19 g, 1.2 mmol) and the mixture was stirred at 80° C. for 20 minutes. To the reaction mixture was added water, and the solution was extracted three times with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate and the organic solvent was removed under reduced pressure. The residue was purified with silica gel chromatography to give tert-butyl (4R)-4-{[(benzyloxy)carbonyl]amino}pentanoate (3.5 g, 98%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07163936B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-bf3169adf428459bac42baf028eefd8b |
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| Source note | uspto-grants-2007_01 |
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