反应详情

A mixture of 3-fluorobenzene-1,2-diol (5.12 g) and (R*, R*)-(±)-1,4-bis (phenylmethoxy)-2,3-butanediol, bis (4-methylbenzenesulphonate) (24.4 g) was stirred with dimethylformamide (DMF) (160 ml) under a nitrogen stream for 45 min. Anhydrous cesium carbonate (13.0 g) was added and the mixture was heated to 150° under reflux for 18 hours. The dark brown mixture was cooled to 30° and diluted with di-isopropyl ether (370 ml) and water (30 ml). The layers were separated and the aqueous layer was re-extracted with di-isopropyl ether (150 ml and then 100 ml). The extracts were sequentially washed within 1M hydrochloric acid (300 ml), 30% aqueous sodium chloride (100 ml) and were combined and evaporated in vacuo to a dark brown oil (12.6 g) which was dissolved in a light petroleum-dichloromethane (3:1) (40 ml) and chromatographed over Sorbsil (Trade Mark) (126 g) using light petroleum-dichloromethane mixtures of gradually increasing polarity. Combination of appropriate fractions and evaporation of the solvents gave the title compound as a yellow oil (7.0 g), NMR (CDCl3) 2.6-2.8 (10H, m, Ph), 3.18-3.38 (3H, m, 6-H, 7-H, 8-H), 5.32-5.58 (4H, m, CH2Ph), 5.64 (2H, m, 2-H, 3-H), 6.06-6.32 (4H, m, CH2O).

1. temperaturethe mixture was heated to 150°
2. temperatureunder reflux for 18 hours
3. temperatureThe dark brown mixture was cooled to 30°
4. customThe layers were separated
5. extractionthe aqueous layer was re-extracted with di-isopropyl ether (150 ml
6. washThe extracts were sequentially washed within 1M hydrochloric acid (300 ml), 30% aqueous sodium chloride (100 ml)
7. customevaporated in vacuo to a dark brown oil (12.6 g) which
8. dissolutionwas dissolved in a light petroleum-dichloromethane (3:1) (40 ml)
9. customchromatographed over Sorbsil (Trade Mark) (126 g)
10. temperatureof gradually increasing polarity
11. customCombination of appropriate fractions and evaporation of the solvents