1-Hexanethiol → 1-(10-Hexylthiodecyl)-2-p-hydroxyphenylind-1-en-5-ol

HRID 569635

反応式

HRID 569635 の反応式
Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]1[C:20]2[C:15](=[CH:16][C:17]([O:21]C)=[CH:18][CH:19]=2)[CH2:14][C:13]=1[C:23]1[CH:28]=[CH:27][C:26]([O:29]C)=[CH:25][CH:24]=1.[CH2:31]([SH:37])[CH2:32][CH2:33][CH2:34][CH2:35][CH3:36].[H-].[Na+]>CN(C)C=O>[CH2:31]([S:37][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]1[C:20]2[C:15](=[CH:16][C:17]([OH:21])=[CH:18][CH:19]=2)[CH2:14][C:13]=1[C:23]1[CH:24]=[CH:25][C:26]([OH:29])=[CH:27][CH:28]=1)[CH2:32][CH2:33][CH2:34][CH2:35][CH3:36]

参加物

5

反応物 3

HCID 81061-HexanethiolHCID 24758Sodium hydrideHCID 86120592HCID 86120592、化合物

生成物 1

HCID 861205951-(10-Hexylthiodecyl)-2-p-hydroxyphenylind-1-en-5-ol

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
60 °C

実験手順

A solution of 1-(10-bromodecyl)-5-methoxy-2-p-methoxyphenylind-1-ene (0.24 g.) in dimethylformamide (1 ml.) was added to a stirred solution of hexanethiol (0.07 g.) and sodium hydride (0.029 g. of a 50% dispersion in mineral oil from which the oil had been washed with petroleum ether) in dimethylformamide which had been stirred at laboratory temperature under an atmosphere of argon for 15 minutes, and the mixture was heated at 60° C. for 2 hours, cooled and water (5 ml.) was added. The mixture was extracted 3 times with ethyl acetate (5 ml. each time) and the combined extracts were washed with water, dried and evaporated to dryness. The residue was purified by chromatography on a silica gel column using a 1:1 v/v mixture of toluene and petroleum ether (b.p. 60°-80° C.) as eluant. The methoxy groups were removed by treatment with boron tribromide in a similar manner to that decribed in Example 7, and the residue was purified by chromatography on a silica gel column using a 9:1 v/v mixture of toluene and ethyl acetate as eluant. There was thus obtained as an oil 1-(10-hexylthiodecyl)-2-p-hydroxyphenylind-1-en-5-ol, the structure of which was confirmed by proton magnetic resonance and mass spectroscopy.

後処理

  1. washof a 50% dispersion in mineral oil from which the oil had been washed with petroleum ether) in dimethylformamide which
  2. temperaturecooled
  3. additionwater (5 ml.) was added
  4. extractionThe mixture was extracted 3 times with ethyl acetate (5 ml
  5. washeach time) and the combined extracts were washed with water
  6. customdried
  7. customevaporated to dryness
  8. customThe residue was purified by chromatography on a silica gel column
  9. additiona 1:1 v/v mixture of toluene and petroleum ether (b.p. 60°-80° C.) as eluant
  10. customThe methoxy groups were removed by treatment with boron tribromide in a similar manner to
  11. customthe residue was purified by chromatography on a silica gel column
  12. additiona 9:1 v/v mixture of toluene and ethyl acetate as eluant

出典と根拠

ORDレコード
ord-17bf1dff6cf0451197712895890b08f6
出典データセット
uspto-grants-1988_03
特許番号
US04732912

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