반응식
[O:1]=[CH:2][C@H:3]([C@H:5]([C@@H:7]([CH2:9][OH:10])[OH:8])[OH:6])[OH:4].[CH2:11](O)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>C(OCC)C>[O:1]([CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C@H:2]1[O:10][CH2:9][C@@H:7]([OH:8])[C@H:5]([OH:6])[C@@H:3]1[OH:4]참가 물질
4
반응 조건
- 온도
- -5 °C
실험 절차
A mixture of D-lyxose (10 g, 66.6 mmol) and benzyl alcohol (50 ml) was cooled to -5° C. and hydrogen chloride was bubbled through it for 3 to 5 hours while monitoring the reaction on tlc (ethyl acetate-ethyl alcohol 7:1). To this reaction mixture diethyl ether (100 ml) was added with stirring and the mixture was allowed to stand at 5° C. for 12 hours. The crystals were filtered, washed with ether and air dried to give 4 (14.1 g, 88.1%).
후처리
- customhydrogen chloride was bubbled through it for 3 to 5 hours
- customthe reaction on tlc (ethyl acetate-ethyl alcohol 7:1)
- filtrationThe crystals were filtered
- washwashed with ether and air
- customdried
출처 및 근거
- ORD 기록
- ord-f9b7839603514c9d8d055fe2a413cb99
- 출처 데이터셋
- uspto-grants-1998_06
- 특허 번호
- US05773239
연결된 노트
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