Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | (3S)-3-(2-methoxy-2-oxoethyl)-5-methylhexanoic acid | HCID 71697547 | — |
| Product | HCID 24885501 | HCID 24885501 | — |
Reaction Steps
A round-bottomed flask is equipped with magnetic stirrer and charged with methylene dichloride (100 ml), (S)-3-((Methoxycarbonyl)methyl)-5-methylhexanoic acid (20 g) and with triethylamine (0.77 g) and cooled to 0-5° C. followed by addition of ethyl chloroformate (9 g). The mixture was stirred for 1-2 h at a temperature of 20° C. to 25° C., followed by quenching with 25% aqueous ammonia (100 ml). The resulted slurry is filtered and washed with water and dried to obtain a solid of (R)-methyl 3-(carbamoylmethyl)-5-methylhexanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07462738B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-f0ec840affec41828b10b83043b7a585 |
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| Source note | uspto-grants-2008_12 |
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