Water → HCID 21317597、化合物

HRID 65641ノート

反応式

HRID 65641 の反応式
Cl[CH2:2][CH2:3][S:4]([CH:7]([CH2:19][CH2:20][CH2:21][CH:22]([O:28]C(=O)C)[CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]([O:16]CC)=[O:15])(=[O:6])=[O:5].[OH-].[Na+].O>O1CCCC1>[CH:3]([S:4]([CH:7]([CH2:19][CH2:20][CH2:21][CH:22]([OH:28])[CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]([OH:16])=[O:15])(=[O:6])=[O:5])=[CH2:2]

参加物

5

反応物 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 21317539HCID 21317539、化合物

生成物 1

HCID 21317597HCID 21317597、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
25 °C

実験手順

A mixture of ethyl 8-(2-chloroethylsulfonyl)-12-acetoxyheptadecanoate (43.5 g., 0.09 mole), sodium hydroxide (14.4 g., 0.36 mole), water (150 ml.) and tetrahydrofuran (600 ml.) is stirred at 25° C. for 24 hours. Most of the tetrahydrofuran is removed by evaporation in vacuo keeping the temperature of the evaporating solution at 30° C. or below. The residue is diluted with water (300 ml.) and extracted with ether. The aqueous solution is acidified with dilute hydrochloric acid. The oily product is taken up in ether, washed with water and dried over sodium sulfate. The ether is evaporated to leave the product as a yellowish, very viscous oil. Purification is effected by column chromatography on silica gel with benzene-dioxane as eluting solvent mixture. The title compound is obtained as a colorless viscous oil.

後処理

  1. customMost of the tetrahydrofuran is removed by evaporation in vacuo
  2. customat 30° C. or below
  3. additionThe residue is diluted with water (300 ml.)
  4. extractionextracted with ether
  5. washwashed with water
  6. dry with materialdried over sodium sulfate
  7. customThe ether is evaporated
  8. customto leave the product as a yellowish, very viscous oil
  9. customPurification
  10. washas eluting solvent mixture

出典と根拠

ORDレコード
ord-f4c68b35428341e8a9ac28fb4423276c
出典データセット
uspto-grants-1978_12
特許番号
US04128564

反応ノート

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