Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16347생성일: 2026년 10월 24일
Ammonium Chloride → tert-butyl {(S)-1-benzyloxymethyl-2-[2-oxo-2-(3,4,5-trifluorophenyl)ethoxy]ethyl}carbamate
https://huagongshe.com/ko/reaction/16347
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 1-Bromo-3,4,5-trifluorobenzene | HCID 611409 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 반응물 | tert-butyl(S)-3-benzyloxymethyl-5-oxomorpholine-4-carboxylate | HCID 67373012 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | tert-butyl {(S)-1-benzyloxymethyl-2-[2-oxo-2-(3,4,5-trifluorophenyl)ethoxy]ethyl}carbamate | HCID 67373700 | — |
반응 단계
1-Bromo-3,4,5-trifluorobenzene (446 μL) was dropwise added to a diethylether suspension (5 mL) of magnesium (249 mg) over 10 min at 40° C. The resulting reaction solution was stirred at 40° C. for 1 hr and then dropwise added to a tetrahydrofuran solution (30 mL) of (S)-3-benzyloxymethyl-5-oxomorpholine-4-carboxylic acid tert-butyl ester (1.1 g) over 10 min at −40° C. The resulting reaction solution was stirred at −40° C. for 1 hr, and a saturated ammonium chloride aqueous solution was gradually added dropwise thereto at −40° C. The resulting reaction solution was warmed up to room temperature, and then ethyl acetate was added thereto. The organic layer was separated, washed with saturated saline, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (heptane-ethyl acetate system) to give 952 mg of the title compound. The physical property values of this compound were as follows:
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07737141B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-1cfeb729204c45378d4035f81c16e13b |
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| 출처 메모 | uspto-grants-2010_06 |
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