Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 742634생성일: 2026년 10월 26일
Triethylamine → N-methoxyacetyl-2-(3,4-dichlorophenyl)-4-(tetrahydropyran-2-yloxy)butylamin
https://huagongshe.com/reaction/742634
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Methoxyacetic Acid | HCID 12251 | — |
| 반응물 | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| 반응물 | 2-(3-(3,4-Dichlorophenyl)-4-aminobutyl)oxytetrahydropyran | HCID 15670808 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-methoxyacetyl-2-(3,4-dichlorophenyl)-4-(tetrahydropyran-2-yloxy)butylamin | HCID 19705334 | 71.1% |
반응 단계
A mixture of 8.6 g of 2-(3,4-dichlorophenyl)-4-(tetrahydropyran-2-yloxy)butylamine (obtained according to PREPARATION (I), step (b)), 2.46 g of methoxyacetic acid, 5.55 g of triethylamine in 50 ml of dichloromethane is cooled to 0° C. and 14.5 g of BOP is added thereto. The reaction mixture is stirred for one hour at room temperature and concentrated under vacuum. The residue is taken up in ethyl acetate and is successively washed with water, dried over Na2SO4 and concentrated under vacuum. The residue is chromatographed on silica gel using CH2Cl2/CH3OH (100/1 v/v) as the eluent to give 7.5 g of the expected product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05554763 |
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| 출처 데이터셋 | uspto-grants-1996_09 |
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| ORD ID | ord-0c8ce3533d57469fb98ac376e471eabf |
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| 출처 메모 | uspto-grants-1996_09 |
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