반응 #1623

ord-5e96551488e842a0ae7a5944f04ecff0

반응 방정식

CCOP(=O)(COS(=O)(=O)c1ccc(Cl)cc1)OCC
4-chlorobenzenesulfonyloxymethylphosphonate diethyl ester
[H-].[Na+]
sodium hydride
O=C(O)NCCc1ccc(O)cc1
2-(4-hydroxyphenyl)ethylcarbamic acid
O
water
CCOP(=O)(COc1ccc(CCNC(=O)OC(C)(C)C)cc1)OCC
title compound
CCOP(=O)(COc1ccc(CCNC(=O)OC(C)(C)C)cc1)OCC
4-(2-t-Butoxycarbonylaminoethyl)phenoxymethyl phosphonic acid, diethyl ester

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas added
  2. 2
    workup.STIRRINGthe resulting pale yellow solution stirred at room temperature overnight
  3. 3
    추출extracted with diethyl ether/ethyl acetate (1:1, 3×150 ml) and finally ethyl acetate (3×100 ml)
  4. 4
    세척The combined extracts were washed with brine
  5. 5
    건조dried over anhydrous sodium sulfate
  6. 6
    기타evaporated to dryness
  7. 7
    기타The resulting oil was purified by chromatography on silica gel with a gradient of 3:2 pentane

실험 절차

A solution of 2-(4-hydroxyphenyl)ethylcarbamic acid, t-butyl ester1 (4.0 g, 16.9 mMol) in dry DMSO (37.5 ml) was cooled in an ice-bath and treated with sodium hydride (80% in mineral oil 0.557 g, 1.1 equiv) with stirring under argon according to the method described by Cornforth2. When effervescence ceased a solution of 4-chlorobenzenesulfonyloxymethylphosphonate diethyl ester (6.07 g, 1.05 equiv) in dry DMSO (110 ml) was added and the resulting pale yellow solution stirred at room temperature overnight. The mixture was then poured into water (550 ml) and extracted with diethyl ether/ethyl acetate (1:1, 3×150 ml) and finally ethyl acetate (3×100 ml). The combined extracts were washed with brine, dried over anhydrous sodium sulfate and evaporated to dryness. The resulting oil was purified by chromatography on silica gel with a gradient of 3:2 pentane:ethyl acetate rising to 100% ethyl acetate to give the title compound as a colourless viscous oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05726165uspto-grants-1998_03