Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
(+-)-2-Butanol → 2-phenyl-1-(1-phenyl-1H-1,2,3-triazol-5-yl)ethanamine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | (+-)-2-Butanol | HCID 6568 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | 1-phenyl-1H-1,2,3-triazole-5-carbonitrile | HCID 84653709 | — |
| 반응물 | HCID 178418336 | HCID 178418336 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-phenyl-1-(1-phenyl-1H-1,2,3-triazol-5-yl)ethanamine | HCID 90281247 | — |
반응 단계
To a solution of 9C (280 mg, 1.63 mmol) in tetrahydrofuran (5 mL), benzylmagnesium chloride (2M in THF) (1.23 mL, 2.46 mmol) was added dropwise. After 3 hours, 3 mL of 2-butanol was added to the reaction and sodium borohydride (0.5 g) was added to the mixture by portion. The reaction was monitored by LC/Mass until it was done. Methanol (5 mL) was added to the mixture. The organic layer was washed with brine and extracted with ethyl acetate (50 mL twice). The organic layer was dried with Na2SO4, filtered and concentrated. The crude product was purified by flash column (Rf: 0.3, 3% MeOH/DCM) to provide the desired product. MS (m/z) 265 [M+H]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09220710B2 |
| 출처 데이터셋 | uspto-grants-2015_12 |
| ORD ID | ord-55b96b07b7ae4eed898402a7696ec0dc |
| 출처 메모 | uspto-grants-2015_12 |