HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648377Generated: November 1, 2026
Ethyl chloroformate → EtOCO-D,L-Phe(alphaMe)-OH
https://huagongshe.com/reaction/1648377
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | DL-alpha-Methylphenylalanine | HCID 108055 | — |
| Reactant | N,O-bis(trimethylsilyl)acetamide | HCID 6913588 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | EtOCO-D,L-Phe(alphaMe)-OH | HCID 20192757 | 98% |
Reaction Steps
To a stirring suspension of D,L-Phe(αMe)-OH (7.5 g, 42 mmol) in tetrahydrofuran (250 mL) was added N,O-bis(trimethylsilyl)acetamide (12.8 g, 62.8 mmol). Upon clarification the solution was cooled to 0° C. and N,N-diisopropylethylamine (5.4 g, 42 mmol) was added, followed by ethyl chloroformate (4.5 g, 42 mmol). After 2 h, water (100 mL) was added and then the organic solvent was removed in vacuo. The aqueous phase was diluted with 1N NaOH and washed twice with diethyl ether. The aqueous phase was then acidified to pH 2 with concentrated HCl and extracted three times with ethyl acetate. The combined ethyl acetate extracts were dried (Na2SO4), filtered and concentrated in vacuo to give 10.3 g (98% yield) of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05436229 |
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| Source dataset | uspto-grants-1995_07 |
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| ORD ID | ord-7656687a574b4fa383524df790d8c9f3 |
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| Source note | uspto-grants-1995_07 |
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