Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 499725생성일: 2026년 10월 27일
Cyclohexane → 3,4,5-Tris-benzyloxy-6-benzyloxymethyl-2-(2,5-bis(trityloxymethyl)phenyl)tetrahydropyran-2-ol
https://huagongshe.com/reaction/499725
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cyclohexane | HCID 8078 | — |
| 반응물 | 3,4,5-Tribenzyloxy-6-(benzyloxymethyl)tetrahydropyran-2-one | HCID 4585508 | — |
| 반응물 | 2-Bromo-1,4-bis(trityloxymethyl)benzene | HCID 68458085 | — |
| 반응물 | CID 53628100 | HCID 178418400 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 3,4,5-Tris-benzyloxy-6-benzyloxymethyl-2-(2,5-bis(trityloxymethyl)phenyl)tetrahydropyran-2-ol | HCID 78088908 | 80.1% |
반응 단계
Under a nitrogen stream, to a solution of 2-bromo-1,4-bis(trityloxymethyl)benzene (255.3 mg, 0.36 mmol) in toluene (1.5 ml), a cyclohexane solution of sec-butyllithium (0.99 M, 367 μl, 0.36 mmol) was added dropwise at room temperature and the solution was stirred for 30 minutes. This solution was added dropwise at −78° C. to a solution of 3,4,5-trisbenzyloxy-6-(benzyloxymethyl)tetrahydropyran-2-one (140 mg, 0.26 mmol) in toluene (1.5 ml) and the mixture was stirred at the same temperature for 30 minutes. After addition of water, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and then evaporated under reduced pressure to remove the solvent. The resulting residue was purified by silica gel column chromatography (developing solution=ethyl acetate:n-hexane (1:5)) to give the titled compound (242 mg, 80%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07767651B2 |
|---|
| 출처 데이터셋 | uspto-grants-2010_08 |
|---|
| ORD ID | ord-4fb96350c384456ebcf449f9b89690e7 |
|---|
| 출처 메모 | uspto-grants-2010_08 |
|---|