反応 #2716

ord-9f2a11bfe87a4bf99972d2587a25f59f

反応方程式

CN(C)C=O
DMF
Cc1ccc(C2=CC(C)(C)Oc3ccc(Br)cc32)s1
2,2-dimethyl-4(5-methyl-thien-2-yl)-6-bromo-chrom-3-ene
Cc1ccc(C2=CC(C)(C)Oc3ccc(Br)cc32)s1
Compound R
Cc1ccc(C2=CC(C)(C)Oc3ccc(Br)cc32)s1
2,2-dimethyl-4(5-methyl-thien-2-yl)-6-bromo-chrom-3-ene
[Li][C](C)(C)C
t-BuLi
Cc1ccc(C2=CC(C)(C)Oc3ccc(C=O)cc32)s1
title compound
Cc1ccc(C2=CC(C)(C)Oc3ccc(C=O)cc32)s1
2,2-Dimethyl-4(5-methyl-thien-2-yl)-chrom-3-en-6-al

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    洗浄washed with brine (10 mL)
  2. 2
    その他dried
  3. 3
    その他the solvent was removed by evaporation
  4. 4
    その他Purification by chromatography on silica gel column

実験手順

To a cold (-78° C.) solution of 2,2-dimethyl-4(5-methyl-thien-2-yl)-6-bromo-chrom-3-ene (Compound R, 1.2 g, 3.6 mmol) in THF (10 mL), was added t-BuLi in pentane (1.7M solution, 2.3 mL). After 30 minutes, DMF (465 mg, 5 mmol) was added and the mixture was allowed to warm to ambient temperature and stirred for 3 hours. The mixture was diluted with ethyl acetate (150 mL), washed with brine (10 mL), dried and the solvent was removed by evaporation. Purification by chromatography on silica gel column gave the title compound as a colorless oil.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05728846uspto-grants-1998_03