Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1611742생성일: 2026년 10월 27일
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → (S)-3-(t-butyldimethylsilyloxy)-5-phenyl-pentan-1-ol
https://huagongshe.com/reaction/1611742
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | (S)-3-(t-butyldimethylsilyloxy)-5-(4-methoxy-benzyloxy)-1-phenyl pentane | HCID 69589755 | — |
| 용매 | Water methylene chloride | HCID 21908982 | — |
| 생성물 | (S)-3-(t-butyldimethylsilyloxy)-5-phenyl-pentan-1-ol | HCID 69589993 | 99.4% |
반응 단계
(S)-3-(t-butyldimethylsilyloxy)-5-(4-methoxy-benzyloxy)-1-phenyl pentane (15 g, 36.2 mmol) was dissolved in a solvent mixture of dichloromethane-water (20:1) (252 ml) DDQ (8.2 g, 36.2 mmol) was added thereto and the mixture was stirred for 30 minutes at room temperature. After completion of the reaction, saturated aqueous NaHCO3 solution (100 ml) was added to the reaction solution to stop the reaction. The organic layer was separated and the aqueous layer was extracted with dichloromethane. The organic layers were combined, washed with saturated aqueous NaHCO3 solution and saturated aqueous NaCl solution, dried over MgSO4, filtered, and concentrated. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=15:1) to give (S)-3-(t-butyldimethylsilyloxy)-5-phenyl-pentan-1-ol (10.6 g, Yield 99%) of a yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06989458B2 |
|---|
| 출처 데이터셋 | uspto-grants-2006_01 |
|---|
| ORD ID | ord-76fadddb889c48e281915b234f36a60a |
|---|
| 출처 메모 | uspto-grants-2006_01 |
|---|