Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 747733생성일: 2026년 10월 25일
4-Methylmorpholine → N-((1,1-Dimethylethoxy)carbonyl)-4-iodo-D-phenylalanine methyl ester
https://huagongshe.com/reaction/747733
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Methylmorpholine | HCID 7972 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | 4-Iodo-D-phenylalanine | HCID 2733279 | — |
| 반응물 | Carbonic acid, bis(1,1-dimethylethyl) ester | HCID 10219638 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-((1,1-Dimethylethoxy)carbonyl)-4-iodo-D-phenylalanine methyl ester | HCID 53885913 | — |
반응 단계
17 ml (230 mmol) of thionyl chloride was added to 3 ml of methanol under cooling with ice. 22.2 g (76.3 mmol) of D-4-iodophenylalanine was added to the resultant mixture, and they were heated under reflux for 2 hours. The solvent was evaporated. 15 ml (137 mmol) of N-methylmorpholine, 12 g (55 mmol) of di-t-butyl carbonate and 100 ml of dichloromethane were added to the residue, and they were stirred for 19 hours. The reaction liquid was diluted with water. After the extraction with dichloromethane, the organic layer was successively washed with saturated aqueous sodium hydrogencarbonate solution and saturated aqueous NaCl solution, and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by the silica gel column chromatography to obtain the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07396844B1 |
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| 출처 데이터셋 | uspto-grants-2008_07 |
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| ORD ID | ord-a188eb4a90d0445e998d98b4356b3a26 |
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| 출처 메모 | uspto-grants-2008_07 |
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