Hydrogen Peroxide → (-)-cis-Myrtanol
반응식
B.C(SCCC(C)C)CC(C)C.CC1(C)[C@H]2C[C@@H]1CCC2=C.[OH-].[Na+].OO.C(=O)([O-])[O-].[K+].[K+].C(SCCC(C)C)CC(C)C.[CH3:44][C:45]1([CH3:54])[C@@H:50]2[CH2:51][C@H:46]1[CH2:47][CH2:48][C@@H:49]2[CH2:52][OH:53]>C1COCC1>[CH3:44][C:45]1([CH3:54])[C@H:50]2[CH2:51][C@@H:46]1[CH2:47][CH2:48][C@H:49]2[CH2:52][OH:53]참가 물질
반응물 7
생성물 1
시약·촉매·용매 1
실험 절차
Borane-diisoamyl sulfide (5.0 ml, 21 mmol) was dissolved in THF (20 ml) and (-)-β-pinene (8.86 g, 64 mmol), [α]23D=-20.8° (neat), 91% ee, was added at 0° C. The mixture was kept at room temperature for 1 h and oxidized by the addition of 3M sodium hydroxide (10 ml, 30 mmol) and 30% hydrogen peroxide (7 ml, 70 mmol) keeping the temperature during the addition below 30° C. and then stirring at room temperature for 3 h. The mixture was saturated with potassium carbonate, the THF layer was separated and the aqueous layer was extracted with diethyl ether (2×50 ml). The extracts were combined with the THF solution, dried over magnesium sulfate and distilled using a Widmer column to give a first fraction, 4.25 g, bp 45°-58° C./0.1 mm Hg composed of diisoamyl sulfide (77%) and cis-myrtanol (23%) and a second fraction 7.96 g (82%), bp 58°-60° C./0.1 mm Hg, n20D=1.4907, [α]°D=-19.4° (neat).
후처리
- additionduring the addition below 30° C.
- customthe THF layer was separated
- extractionthe aqueous layer was extracted with diethyl ether (2×50 ml)
- dry with materialdried over magnesium sulfate
- distillationdistilled
- customto give a first fraction, 4.25 g, bp 45°-58° C./0.1 mm Hg
- customn20D=1.4907, [α]°D=-19.4° (neat)
출처 및 근거
- ORD 기록
- ord-ed64b13e10ef4a3293adf617ddbf550e
- 출처 데이터셋
- uspto-grants-1996_10
- 특허 번호
- US05567849
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