반응 #1552075
ord-f0c66e45f9c7415f904df9a6d9e8ad36
반응 방정식
반응 조건
후처리
- 1workup.STIRRINGthe suspension stirred for 30 min
- 2기타to return to room temperature
- 3workup.STIRRINGAfter stirring for a further 3 h
- 4기타the reaction crude
- 5workup.ADDITIONwas poured onto brine (400 ml)
- 6workup.STIRRINGstirred for 10 min
- 7기타to separate
- 8추출The upper aqueous phase was extracted with methylene chloride (150 ml)
- 9건조dried (Na2SO4)
- 10농축concentrated in vacuo
실험 절차
4-Isobutyl-6-methylcyclohex-3-enecarbaldehyde 3b (8 g, 44 mmol) was dissolved in methylene chloride (400 ml) and cooled to −3° C. with stirring and under nitrogen. KOtBu (6.7 g, 58 mmol) and MeI (19 g, 130 mmol) were added sequentially and the suspension stirred for 30 min before being allowed to return to room temperature. After stirring for a further 3 h the reaction crude was poured onto brine (400 ml), stirred for 10 min and the phases allowed to separate. The upper aqueous phase was extracted with methylene chloride (150 ml) and the organic phases combined, dried (Na2SO4) and concentrated in vacuo to give 8.5 g of an orange oil (8.5 g). The oil was purified by flash chromatography (MTBE/hexane 1:9) and combination of pure fractions gave 3c as a 7:3 mixture of diastereomers (7 g, colorless oil, 80% yield). 1 g of the oil was distilled to give a sample for olfactory assessment. (0.52 g, colourless oil, >99% pure).