HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823823Generated: October 25, 2026
Benzyl chloroformate → HCID 20681205, compound
https://huagongshe.com/reaction/1823823
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | 2-Methylglutamic acid | HCID 95440 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 20681205 | HCID 20681205 | 83% |
Reaction Steps
To a stirred solution of α-methyl-D,L-glutamic acid (10 g, 62 mmol) in 2 N sodium hydroxide (62 mL) at 0–5° C. was added benzyl chloroformate (12.7 g, 74.4 mmol) over 30 min. After the addition was complete the reaction mixture was stirred at room temperature for 3 hours. During this time the pH was maintained at 11 by addition of 2 N sodium hydroxide (33 mL). The reaction mixture was then extracted with ether (60 mL). The aqueous layer was cooled in an ice bath and then acidified with 4N hydrochloric acid (34 mL) to pH=1. The resulting mixture was extracted with ethyl acetate (3×100 mL). The combined ethyl acetate extracts were washed with brine (60 mL) and dried (MgSO4). The solvent was removed in vacuo to give 15.2 g (83%) of N-benzyloxycarbonyl-α-methylglutamic acid as an oil: 1H NMR (CDCl3) δ 8.73(m, 5H), 5.77(b, 1H), 5.09(s, 2H), 2.45–2.27(m, 4H), 2.0(s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07041680B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-618e90e4302a42f5a75fc0e505246df7 |
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| Source note | uspto-grants-2006_05 |
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