HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638119Generated: October 25, 2026
Benzyl chloroformate → N-(Benzyloxycarbonyl)-D-phenylalanine
https://huagongshe.com/reaction/638119
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | D-Phenylalanine | HCID 71567 | — |
| Product | N-(Benzyloxycarbonyl)-D-phenylalanine | HCID 675678 | — |
Reaction Steps
A 15.0 g sample of D-phenylalanine was dissolved in 45 ml of aqueous solution containing 7.26 g of 50% sodium hydroxide. This solution was stirred at 0°-10° C. as 16.3 g of benzyl chloroformate was added rapidly in portions. The resulting reaction was mildly exothermic, and shortly after addition, solids precipitated. An additional 45 ml of water and 3.63 g of 50% sodium hydroxide were added, causing most of the solids to redissolve. The reaction mixture was stirred for 20 minutes and then acidified with 6N hydrochloric acid. The resulting solids were filtered, washed with water and then with hexane, and dried by suction and then under vacuum to give 47 g of white solids. These solids dissolved in ether were washed twice with 1N hydrochloric acid and then with water, dried over MgSO4 and stripped to 35° C. at 2.5 mm Hg to give 27.7 g of the desired product as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04560515 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-75d049a89e8c46a88c7ef5ebbd9887a3 |
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| Source note | uspto-grants-1985_12 |
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