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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1374135생성일: 2026년 10월 25일

HCID 178418361, 화합물 → Carnosine

https://huagongshe.com/reaction/1374135

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참여 물질

역할이름HCID투입량
반응물HCID 178418361HCID 178418361—
반응물HCID 178511198HCID 178511198—
촉매RhodiumHCID 23948—
용매AmmoniaHCID 222—
용매MethanolHCID 887—
생성물CarnosineHCID 439224—

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온도90 °C

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A 1-litre pressure autoclave was initially charged with 1.76 g of Rh/C (0.4 mol % pure Rh, based on reactant used) in a mixture of 94.2 g of ammonia solution (25% in H2O) and 62.8 g of methanol. The autoclave was closed, and the contents were heated to 90° C. and the autoclave was pressurized with 40 bar of hydrogen. A, solution of 20.0 g (0.09 mol) of (S)-2-(cyanoacetyl-amino)-3-(1H-imidazol-4-yl)propionic acid (prepared according to Example 3) in a mixture of 94.2 g of ammonia solution (25% in H2O) and 62.8 g of methanol was then metered in over the course of one hour. After further reaction at 90° C. for one hour, the reaction mixture was cooled to room temperature. The autoclave was depressurized and the catalyst was filtered off via activated carbon. An in-process HPLC analysis showed that the clear greenish reaction solution (326.2 g) contained 5.74% (m/m) carnosine, corresponding to a selectivity of 92% for complete conversion. The reaction mixture was then concentrated to approx. 60 g in a rotary evaporator. Dropwise addition of 174 g of ethanol caused precipitation of a white solid which was filtered off and dried at 50° C./20 mbar.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07164028B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-f7bc1063fa2a4b8494d08df11f44732e
출처 메모uspto-grants-2007_01