Coumarin → 2,2-Dimethyl-6-Chromanesulfonyl Chloride

温度

5 °C

A solution of 2,2-dimethylchroman [obtained by an analogous procedure to that described in Chem. Ber., 1904, 37, 494, for the preparation of 2,2-dimethyl-2H-chromene, but using dihydrocoumarin as starting material in place of coumarin] (50 g, 308 mM) in dichloromethane (250 ml) was added dropwise to a solution of chlorosulphonic acid (40 ml, 602 mM) and phosphorus pentachloride (50 g, 204 mM) in dichloromethane (250 ml), cooled to 5° C. under an atmosphere of argon. The colour of the solution changed from pale yellow to orange. When the addition was complete, the mixture was slowly allowed to attain ambient temperature and stirred for 2 hours. The reaction mixture was poured onto ice-water and the organic phase was separated. The aqueous layer was extracted with dichloromethane (3×20 ml), and the combined organic extracts were washed with water and dried (MgSO4). The solvent was removed by evaporation to give 2,2-dimethylchroman-6-sulphonyl chloride as a pale purple solid (42.6 g, 53% yield), m.p. 89°-92° C. (after recrystallisation from hexane).

1. additionWhen the addition
2. customto attain ambient temperature
3. additionThe reaction mixture was poured onto ice-water
4. customthe organic phase was separated
5. extractionThe aqueous layer was extracted with dichloromethane (3×20 ml)
6. washthe combined organic extracts were washed with water
7. dry with materialdried (MgSO4)
8. customThe solvent was removed by evaporation
9. customto give

ORDレコード

ord-ce3eb3a6bc334783bb2c273a209def75

出典データセット

uspto-grants-1993_02

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05185452