HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79704Generated: October 26, 2026
Diisobutylaluminum hydride → 2,2-Bis(tert-butoxycarbonylamino)-5-oxo-pentanoic acid benzyl ester
https://huagongshe.com/reaction/79704
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | 2,2-Bis(tert-butoxycarbonylamino)-4-(methoxy-methyl-carbamoyl)-butyric acid benzyl ester | HCID 86648875 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2,2-Bis(tert-butoxycarbonylamino)-5-oxo-pentanoic acid benzyl ester | HCID 86648876 | 75.2% |
Reaction Steps
A solution of DIBAL (1.0 M, 14.7 mL, 14.7 mmol) in hexane was added dropwise to a solution of 2,2-bis(tert-butoxycarbonylamino)-4-(methoxy-methyl-carbamoyl)-butyric acid benzyl ester (4 g, 10.5 mmol) under an atmosphere of nitrogen at −78° C. After 2 hours the mixture was quenched with saturated ammonium chloride (30 mL) and allowed to warm to room temperature. Water (20 mL) was added, and the mixture was extracted with diethyl ether (3×50 mL). The combined organic phases were left to stand at room temperature for 15 minutes. The resulting thick gel was filtered through a pad of CELITE. The filtrate was dried over sodium sulfate, filtered and the solvent was removed under reduced pressure to provide 2,2-bis(tert-butoxycarbonylamino)-5-oxo-pentanoic acid benzyl ester (3.34 g, 7.9 mmol, 75%). This was used immediately in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841278B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-e871b63dd63f41828df9a0e18ab0dd26 |
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| Source note | uspto-grants-2014_09 |
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