Triethylamine → HCID 86742997、化合物

HRID 1761771ノート

反応式

HRID 1761771 の反応式
[OH:1][CH2:2]/[CH:3]=[C:4](/[CH3:17])\[CH2:5][CH2:6]/[CH:7]=[C:8](\[CH3:16])/[CH2:9][CH2:10][C:11](=[O:15])[C:12]([CH3:14])=[CH2:13].[C:18]([O:22][CH3:23])(=[O:21])[CH2:19][SH:20].C(N(CC)CC)C>CO>[OH:1][CH2:2]/[CH:3]=[C:4](/[CH3:17])\[CH2:5][CH2:6]/[CH:7]=[C:8](\[CH3:16])/[CH2:9][CH2:10][C:11](=[O:15])[CH:12]([CH3:14])[CH2:13][S:20][CH2:19][C:18]([O:22][CH3:23])=[O:21]

参加物

5

反応物 3

HCID 8471TriethylamineHCID 16907Methyl ThioglycolateHCID 86742985HCID 86742985、化合物

生成物 1

HCID 86742997HCID 86742997、化合物

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A solution of 4 g (0.0017 mol) of (6E,10Z)-12-hydroxy-2,6,10-trimethyl-1,6,10-dodecatrien-3-one in 13 ml of methanol is treated with 4.7 ml of methyl thioglycolate and 7.1 ml of triethylamine. The solution is stirred at room temperature for 18 hours under argon. After removing the solvent the residue is worked-up with water and methylene chloride. The organic phase is dried and freed from solvent. The residue is chromatographed on silica gel with ether. There is obtained methyl [[(6E,10Z)-12-hydroxy-2,6,10-trimethyl-3-oxo-6,10-dodecadienyl]thio]acetate which has the following bands in the IR spectrum: 1736 cm-1, 1711 cm-1, 1437 cm-1, 1408 cm-1, 1281 cm-1, 1137 cm-1, 1007 cm-1.

後処理

  1. customAfter removing the solvent the residue
  2. customThe organic phase is dried
  3. customThe residue is chromatographed on silica gel with ether

出典と根拠

ORDレコード
ord-f34b58e2b3404d59bd5461c72ed7371a
出典データセット
uspto-grants-1989_05
特許番号
US04827004

反応ノート

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