HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430945Generated: October 30, 2026
Benzyl chloroformate → HCID 131720810, compound
https://huagongshe.com/reaction/430945
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 14503313 | HCID 14503313 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131720810 | HCID 131720810 | 92% |
Reaction Steps
To a solution under an atmosphere of nitrogen containing 1.0 g (6.8 mmol) of 3-(S)-amino-2-(R,S)-hydroxy-4-methylpentanoic acid in 9.5 ml, of 1 N NaOH and 10 mL of dioxane was added 1.43 g (8.4 mmol) of benzyl chloroformate. The pH was maintained above pH 8 with 1 N NaOH as needed. The reaction mixture was allowed to stir at room temperature overnight. The reaction was diluted with water and washed with ether. The aqueous layer was acidified with 1 N HCl to pH=2 and extracted with ether (2×). The combined organic layers were dried over magnesium sulfate, filtered and evaporated in vacuo to afford 1.75 g (92%) of 3-(S)-[(benzyloxycarbonyl)amino]-2-(R,S)-hydroxy-4-methylpentanoic acid as a light yellow viscous oil. FAB MS [M+H]m/z; Calcd: 282, Found: 282.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06656911B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-92d32f47746d4f13a712738427e173af |
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| Source note | uspto-grants-2003_12 |
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