Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
N-(3-formylphenyl)methanesulfonamide → [3-(Hydroxyethyl)phenyl](methylsulfonyl)amine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | N-(3-formylphenyl)methanesulfonamide | HCID 2794787 | — |
| 반응물 | HCID 178418573 | HCID 178418573 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | [3-(Hydroxyethyl)phenyl](methylsulfonyl)amine | HCID 43508614 | — |
반응 단계
Under argon and at 0° C., 83 mg (0.417 mmol) of N-(3-formylphenyl)methanesulfonamide (Example 86A) were initially charged in 1 ml of abs. tetrahydrofuran. At 0° C., 99 mg (0.833 mmol) of methylmagnesium bromide (3 M in diethyl ether) were added dropwise (resulting in the formulation of a precipitate), and the reaction solution was stirred at this temperature for 2 h. The reaction solution was quenched with water and extracted three times with ethyl acetate. The combined organic phases were dried over sodium sulfate, filtered and evaporated.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09187428B2 |
| 출처 데이터셋 | uspto-grants-2015_11 |
| ORD ID | ord-9ebb46efaf6049d5b841395a69ffd1af |
| 출처 메모 | uspto-grants-2015_11 |