HRID443737

反应详情

EQUATION

反应方程式

HRID 443737 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
65 °C

PROCEDURE

实验过程

A solution of 74.5 g. (0.4 mole) of 1-naphthyl acetic acid, 111.0 g. (0.45 mole) of EEDQ and 66.0 g. (0.4 mole) of α-(1-amino-1-methylethyl)benzenemethanol in 1 l. tetrahydrofuran is stirred and heated for 2 hours at 65° C. and then allowed to stand for 20 hours at room temperature. THF is evaporated in vacuo, and the residue is taken up with ice and 10% aqueous H2SO4 solution to pH 2. The resulting amide is extracted twice with 750 ml. ethyl acetate. The combined organic extracts are washed with 500 ml. dilute NaHCO3, dried (Na2SO4) and evaporated to dryness in vacuo. The oil is dissolved in 1 l. hot isopropyl ether and on standing at 25° C. gives 101.0 g. (77% yield) of N-(2-hydroxy-1,1-dimethyl-2-phenylethyl)-1-naphthaleneacetamide as an off-white crystalline solid of analytical purity, m.p. 106°-107° C.

WORKUP

后处理

  1. customTHF is evaporated in vacuo
  2. extractionThe resulting amide is extracted twice with 750 ml
  3. washThe combined organic extracts are washed with 500 ml
  4. dry with materialdilute NaHCO3, dried (Na2SO4)
  5. customevaporated to dryness in vacuo
  6. dissolutionThe oil is dissolved in 1 l
  7. customon standing at 25° C.
  8. customgives 101.0 g