HRID247561

反应详情

EQUATION

反应方程式

HRID 247561 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A solution of 3.40 g (20.0 mmol) of bis(trimethylsilyl)acetylene and 4.03 g (15.0 mmol) of 3,5-di-t-butyl-4-hydroxybenzoyl chloride [which is prepared from 3,5-di-t-butyl-4-hydroxybenzoic acid by treatment with oxalyl chloride (benzene, 60°, 2h)] in 80 mL of methylene chloride is treated at -78° with 1.78 mL (16.5 mmol) of titanium tetrachloride. The resulting dark mixture is stirred at -78° for 30 minutes and then is allowed to warm to 0° and stirred for an additional 30 minutes. The reaction solution is poured into 3N HCl and the layers are separated. The aqueous portion is extracted with pentane and the combined organic phase is washed with sat. NaCl and dried (MgSO4). The crude silylacetylene intermediate is concentrated, dissolved in 100 mL of methanol and then is treated at room temperature with 20 mL of 0.01M borax. After stirring the mixture at 25° overnight, it is poured into 3N HCl and the aqueous layer is extracted with pentane. The combined organic phase is washed with sat. NaCl and dried (MgSO4). Recyrstallization from hexane affords 2.40 g (62%) of the title compound: mp 100°-101°; IR (CCl4) 3620(s), 3300(m), 2950(s), 2090(m), 1640(s), 1580(s), 1290(s), 1215(vs) cm-1 ; 1H-NMR (CDCl3)δ(ppm) 1.45(s, 18H), 3.30(s, 1H), 5.80(s, 1H), 8.00(s, 2H); 13C-NMR (CDCl3)δ30.09, 34.41, 79.84, 80.80, 127.76, 128.51, 136.34, 160.02, 176.67 ppm.

WORKUP

后处理

  1. temperatureto warm to 0°
  2. stirringstirred for an additional 30 minutes
  3. customthe layers are separated
  4. extractionThe aqueous portion is extracted with pentane
  5. washthe combined organic phase is washed with sat. NaCl
  6. dry with materialdried (MgSO4)
  7. concentrationThe crude silylacetylene intermediate is concentrated
  8. dissolutiondissolved in 100 mL of methanol
  9. additionis treated at room temperature with 20 mL of 0.01M borax
  10. stirringAfter stirring the mixture at 25° overnight, it
  11. additionis poured into 3N HCl
  12. extractionthe aqueous layer is extracted with pentane
  13. washThe combined organic phase is washed with sat. NaCl
  14. dry with materialdried (MgSO4)