تفاعل #53851

ord-6a4da753f0934d5d96db989d8fb86b84

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصAfter extraction with aqueous 10% KHSO4/Et2O (3×)
  2. 2
    غسيلthe organic phases were washed with aqueous saturated NaHCO3 (2×), aqueous 10% NaCl
  3. 3
    تجفيفdried over Na2SO4
  4. 4
    أخرىevaporated

الإجراء التجريبي

A solution of 645 mg (corresponds to 1.65 mmol) of trans-[4-(2-Hydroxy-ethylsulfanylmethyl)-cyclohexyl]-methyl-carbamic acid 4-chloro-phenyl ester in 12 ml CH2Cl2 was treated at 0° C. with 0.14 ml (1.82 mmol) methanesulfonylchloride, 0.20 ml (2.45 mmol) pyridine and 202 mg (1.65 mmol) DMAP. The reaction mixture was warmed up over night to room temperature. Water (2 ml) was added and the reaction was stirred for 5 min. After extraction with aqueous 10% KHSO4/Et2O (3×), the organic phases were washed with aqueous saturated NaHCO3 (2×), aqueous 10% NaCl, dried over Na2SO4 and evaporated to yield 650 mg (quantitative) trans-[4-(2-Chloro-ethylsulfanylmethyl)-cyclohexyl]-methyl-carbamic acid 4-chloro-phenyl ester, MS: 376 (MH+, 2Cl).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06858651B2uspto-grants-2005_02