Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ammonia → (3-((Tert-butyldimethylsilyloxy)methyl)phenyl)methanol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ammonia | HCID 222 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| 반응물 | 1,3-Benzenedimethanol | HCID 69374 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (3-((Tert-butyldimethylsilyloxy)methyl)phenyl)methanol | HCID 10658493 | 45.4% |
반응 단계
To 1,3-benzenedimethanol (5.10 g, 36.91 mmol) in dichloromethane (70 ml) was added at 0° C. triethylamine (7.47 g, 73.82 mmol), 4-dimethyl-aminopyridine (451 mg, 3.61 mmol) and t-butyldimethylchlorosilane (5.56 g, 36.91 mmol) successively, and the mixture was stirred for 20 hours at room temperature. Thereto was added a saturated ammonia solution and the mixture was extracted with ethyl acetate and separated by a separating funnel. The organic layer was washed with water and saturated brine, dried over magnesium sulfate and filtered. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography to give the subject compound (4.23 g, 45%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07781479B2 |
| 출처 데이터셋 | uspto-grants-2010_08 |
| ORD ID | ord-50fc8bbb3b3b47048f33b51ad57a2c25 |
| 출처 메모 | uspto-grants-2010_08 |