참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Benzylamine | HCID 7504 | — |
| 반응물 | [3-(Bromomethyl)oxetan-3-yl]methanol | HCID 529264 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | [1-Benzyl-3-(hydroxymethyl)azetidin-3-YL]methanol | HCID 20164320 | — |
반응 단계
18.1 g of 1A and 11.7 g of benzylamine were mixed with 5 ml of water and the resulting mixture was stirred at 100° C. After 4 hours the solution was allowed to cool to ambient temperature and 13.8 ml of 36% (w/w) hydrochloric acid was added. The resulting mixture was stirred at 60° C. After 2 hours the solution was again allowed to cool to room temperature and then washed with dichloromethane to remove by-products. The aqueous layer was made alkaline by the addition of a solution of 5.5 g of sodium hydroxide in 10 ml of water and stirred at 100° C. for 1 hour. After cooling to ambient temperature the pH of the mixture was raised by addition of another solution of 5.5 g of sodium hydroxide in 10 ml of water and washed with hexane to remove benzylamine. The water was evaporated under reduced pressure, and the solid residue was taken up in dichloromethane. Inorganic salts, which remained undissolved, were removed by filtration, and the dichloromethane was evaporated in vacuo, leaving 1, as a white crystalline solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04665197 |
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| 출처 데이터셋 | uspto-grants-1987_05 |
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| ORD ID | ord-c4cd9b50b8c84c5e8537f76c629da15e |
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| 출처 메모 | uspto-grants-1987_05 |
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