HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981857Generated: November 2, 2026
Benzyl chloroformate → N-(Benzyloxycarbonyl)-D-phenylalanine
https://huagongshe.com/reaction/1981857
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 6 N 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 1 N 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 | US04594196 |
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| Source dataset | uspto-grants-1986_06 |
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| ORD ID | ord-8e09b9eaa99f409dbcf8ac422f270703 |
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| Source note | uspto-grants-1986_06 |
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