反应 #502079
ord-d585f4bc23f648108be1ba6daa57700a
反应方程式
反应物
试剂
反应条件
后处理
- 1其他fitted with condenser
- 2温度The flask was cooled to <10° C.
- 3温度whilst maintaining a temperature of <10° C
- 4workup.STIRRINGas stirred for 2 hours at <10° C
- 5温度cooling
- 6其他The crude reaction mixture
- 7萃取was extracted into methyltert-butyl ether (2×300 mL)
- 8洗涤the organic phase washed with water (200 mL)
- 9干燥The organic phase was dried over magnesium sulphate
- 10过滤filtered
- 11其他the solvent removed by evaporation
实验过程
Tetrahydrofuran (600 mL) was charged to 2 L flask fitted with condenser, nitrogen, thermocouple and mechanical stirrer. The flask was cooled to <10° C. and the flask was inerted with dry nitrogen fed a slow rate. Aluminium chloride (112 g, 840 mmol) was slowly added to the reaction flask whilst maintaining a temperature of <10° C. Then lithium aluminium hydride powder (15.9 g, 420 mmol) was added slowly over 30 minutes. The reaction mixture was stirred for a further 30 minutes at <10° C. To the reaction flask was added slowly a solution of 2-methyl-2-(4-methylpentyl)-1,3-dioxolane (72 g, 420 mmol) in tetrahydrofuran (50 mL) over 30 minutes. The reaction mixtures as stirred for 2 hours at <10° C. Ethyl acetate (200 g) was then added slowly to the reaction mixture to neutralise the excess lithium aluminium hydride—cooling was necessary to counteract the large exotherm. The crude reaction mixture was extracted into methyltert-butyl ether (2×300 mL) and the organic phase washed with water (200 mL). The organic phase was dried over magnesium sulphate, filtered and the solvent removed by evaporation to yield the desired product suitable for the next synthetic step as a colourless oil (100% pure by GC rpa, 70 g, 400 mmol, 96% chemical yield). A small sample was Kugelrohr distilled to give material suitable for olfactive analysis.