تفاعل #2307973
ord-63b32054ba774c74b81fc0406a6cf1e3
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1ترشيحThe mixture was filtered through silica gel
- 2غسيلthe filtrate was washed successively with water, saturated NaHCO3, water and brine
- 3تجفيفThe organics were dried over Na2SO4
- 4ترشيحfiltered
- 5تركيزconcentrated in vacuo to a pale yellow oil
- 6أخرىFinal purification of the crude product
الإجراء التجريبي
A solution of monodispersed ethyl 6-hydroxyhexanoate (50.76 ml, 50.41 g, 227 mmol) in dry dichloromethane (75 ml) was chilled in an ice bath and placed under a nitrogen atmosphere. Triethylamine (34.43 ml, 24.99 g, 247 mmol) was added. A solution of methanesulfonyl chloride (19.15 ml, 28.3 g, 247 mmol) in dry dichloromethane (75 ml) was added dropwise from an addition funnel. The mixture was stirred for three and one half hours, slowly being allowed to come to room temperature as the ice bath melted. The mixture was filtered through silica gel, and the filtrate was washed successively with water, saturated NaHCO3, water and brine. The organics were dried over Na2SO4, filtered and concentrated in vacuo to a pale yellow oil. Final purification of the crude product was achieved by flash chromatography (silica gel, 1/1 hexanes/ethyl acetate) to give the monodispersed compound 2 (46.13 g, 85%) as a clear, colorless oil. FAB MS: m/e 239 (M+H), 193 (M—C2H5O).