참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 4-tert-Butylbenzaldehyde | HCID 70324 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | 2-(4-(Difluoromethoxy)phenyl)ethan-1-amine hydrochloride | HCID 53444441 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | (4-Tert-butyl-benzyl)-[2-(4-difluoromethoxy-phenyl)-ethyl]-amine | HCID 69341978 | 80% |
반응 단계
1.12 ml of 4-tert-butylbenzaldehyde (6.71 mmol), 1 g of 2-(4-difluoromethoxy-phenyl)-ethylamine hydrochloride (4.47 mmol) and 618 mg of potassium carbonate (4.47 mmol) were suspended in 13 ml methanol at rt, and after stirring for 30 min at rt, were refluxed for 2 h. After cooling down to rt, 254 mg (6.71 mmol) sodium borohydride were added and after stirring for 5 min at rt, the reaction mixture was then refluxed for 2.5 h. After cooling down to rt, the reaction mixture was treated with 1.2 ml 1 N HCl and concentrated in vacuo. The residue was diluted with water/EtOAc. After separation of the organic phase, the aqueous phase was extracted with EtOAc and the combined organic phases were washed with brine, dried with magnesium sulfate, filtered off and concentrated in vacuo. The residue was purified by column chromatography (40 g silica gel; EtOAc/heptane 1:4) to give 1.19 g light yellow oil (80%). MS (ISP) 334.3 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07259183B2 |
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| 출처 데이터셋 | uspto-grants-2007_08 |
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| ORD ID | ord-83457a1aaa0b45129d2de660cfba4e43 |
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| 출처 메모 | uspto-grants-2007_08 |
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