反应 #46512

ord-1d39fe7923784c69934bc7c2647b99ac

反应方程式

Cl
HCl
[Cl][Sn]([Cl])([Cl])[Cl]
SnCl4
Cc1cc2ccccc2s1
2-methylbenzo[b]thiophene
COC(Cl)Cl
dichloromethyl methyl ether
Cc1sc2ccccc2c1C=O
title compound
收率 98.2%
Cc1sc2ccccc2c1C=O
2-Methylbenzo[b]thiophene-3-carboxaldehyde
收率 98.2%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONwas poured onto ice water (200 mL)
  2. 2
    workup.STIRRINGstirred until the suspension
  3. 3
    workup.DISSOLUTIONdissolved
  4. 4
    其他The organic phase was separated
  5. 5
    干燥dried (MgSO4)
  6. 6
    浓缩concentrated under vacuum
  7. 7
    其他Purification by flash chromatography on silica gel (10% ethyl acetate/hexane)

实验过程

SnCl4 (20 mL, 67 mmole) was added over 5 min to a stirred solution of 2-methylbenzo[b]thiophene (5.0 g, 33.7 mmole) in CH2Cl2 (75 mL) at 0° C. under argon. After 15 minutes, dichloromethyl methyl ether (3.7 mL, 41 mmole) was added. The reaction became a yellowish colored suspension. The reaction was allowed to warm to RT and stirred for 16 h, then was poured onto ice water (200 mL). The aqueous mixture was acidified with 1.0 N HCl (100 mL) and stirred until the suspension dissolved. The organic phase was separated, dried (MgSO4), and concentrated under vacuum. Purification by flash chromatography on silica gel (10% ethyl acetate/hexane) gave the title compound (5.83 g, 98%) as a white crystalline solid: 1H NMR (400 MHz, CDCl3) δ 10.38 (s, 1 H), 8.61 (d, J=8.1 Hz, 1 H), 7.77 (d, J=8.0 Hz, 1 H), 7.48 (t, 1 H), 7.39 (t, 1 H), 2.93 (s, 3 H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07741339B2uspto-grants-2010_06