Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Dichloromethane → (1R,2R)-2-tert-butyldiphenylsilanyloxy-1-(3,4,5-trifluorophenyl)propylamine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Dichloromethane | HCID 6344 | — |
| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | tert-butyl [(1R,2R)-2-(tert-butyldiphenylsilanyloxy)-1-(3,4,5-trifluorophenyl)propyl]carbamate | HCID 68718850 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | (1R,2R)-2-tert-butyldiphenylsilanyloxy-1-(3,4,5-trifluorophenyl)propylamine | HCID 68719033 | 91.1% |
반응 단계
Trifluoroacetic acid (0.5 mL) was added to a methylene chloride solution (2 mL) of [(1R,2R)-2-tert-butyldiphenylsilanyloxy-1-(3,4,5-trifluorophenyl)propyl]carbamic acid tert-butyl ester (370 mg). This reaction solution was stirred at room temperature for 11 hr. To this reaction solution, a saturated sodium hydrogencarbonate aqueous solution and ethyl acetate were added. The organic layer was separated, washed with a saturated sodium hydrogencarbonate aqueous solution and then with saturated saline. Then, the organic layer was concentrated under reduced pressure to give 275 mg of the title compound. The physical property values of this compound were as follows:
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07737141B2 |
| 출처 데이터셋 | uspto-grants-2010_06 |
| ORD ID | ord-e6ceb06e3c3d40b6964115651d1afece |
| 출처 메모 | uspto-grants-2010_06 |