Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 727126생성일: 2026년 10월 26일
Ethyl bromoacetate → Ethyl beta-tetrahydropyranyloxyethyl-beta-cyano-beta-(3,4-dichlorophenyl)propionate
https://huagongshe.com/reaction/727126
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Ethyl bromoacetate | HCID 7748 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 반응물 | 2-(3-Cyano-3-(3,4-dichlorophenyl)propyl)oxytetrahydropyran | HCID 15670807 | — |
| 생성물 | Ethyl beta-tetrahydropyranyloxyethyl-beta-cyano-beta-(3,4-dichlorophenyl)propionate | HCID 67635049 | — |
반응 단계
21 g of the nitrile prepared above according to (a) are dissolved in 100 ml of tetrahydrofuran, a solution of 0.067 mol of lithium diisopropylamide in 100 ml of tetrahydrofuran is then added dropwise at room temperature and the reaction mixture is stirred for one hour at room temperature. 12 g of ethyl bromoacetate are then added and the mixture is heated at 50° C. for two hours. The mixture is cooled, poured into a saturated solution of ammonium chloride and extracted with ethyl ether, the extract is washed with water and the ether phase is separated off by decantation, dried over Na2SO4 and concentrated under vacuum. The residue is purified by chromatography on silica gel using dichloromethane/ethyl acetate (100/1 v/v) as the eluent. Concentration of the pure fractions gives 13 g of the expected compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05712288 |
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| 출처 데이터셋 | uspto-grants-1998_01 |
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| ORD ID | ord-119f359c15a04becb85497417293de48 |
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| 출처 메모 | uspto-grants-1998_01 |
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