Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2264665생성일: 2026년 10월 25일
Ammonium Chloride → 2-[[2-(3-Benzyloxy-phenyl)-ethyl]-(tetrahydrofuran-3-ylmethyl)amino]-N,N-dimethyl-acetamide hydrochloride
https://huagongshe.com/reaction/2264665
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 3-Furancarboxaldehyde, tetrahydro- | HCID 157568 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | 2-[2-(3-benzyloxy-phenyl)-ethylamino]-N,N-dimethyl-acetamide | HCID 59596856 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 생성물 | 2-[[2-(3-Benzyloxy-phenyl)-ethyl]-(tetrahydrofuran-3-ylmethyl)amino]-N,N-dimethyl-acetamide hydrochloride | HCID 66591206 | 80% |
반응 단계
1.06 g (22 mmol) of NaBH4 were added portionwise to a mixture 2.9 g (9.3 mmol) of 2-[2-(3-benzyloxy-phenyl)-ethylamino]-N,N-dimethyl-acetamide, 1.28 ml (14.1 mmol) of tetrahydrofuran-3-carbaldehyde and 4 g of 4 Å molecular sieves in 130 ml of 1,2-dichloroethane. The reaction mixture was stirred at room temperature overnight. Aqueous ammonium chloride was added, the solvent was removed under vacuum, the residue was extracted with ethyl acetate and the organic phase was washed with an aqueous saturated solution of K2CO3. The solvent was removed under reduced pressure and the product was dissolved in anhydrous an hydrous hydrochloric acid in ethyl acetate. The solvent was removed and the product was triturated with diethyl ether. 3.2 g (80% yield) of the title compound were isolated as a yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07855227B2 |
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| 출처 데이터셋 | uspto-grants-2010_12 |
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| ORD ID | ord-fc38a04f6f0c439a9517ec76642b4e0e |
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| 출처 메모 | uspto-grants-2010_12 |
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