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Acetic Acid → HCID 21398245、化合物

HRID 1439154
ノート
印刷プレビュー

反応式

HRID 1439154 の反応式
[CH3:1][C:2]1[CH:3]=[C:4]([CH:11]=[C:12]([C:15]([CH3:18])([CH3:17])[CH3:16])[C:13]=1[OH:14])[CH2:5][CH2:6][C:7]([O:9][CH3:10])=[O:8].[CH2:19]([S:37][CH2:38][CH:39]([OH:42])CO)[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36].[CH3:43][O-:44].[Na+].[C:46]([OH:49])(=O)[CH3:47]>>[CH2:19]([S:37][CH2:38][CH:39]([O:42][C:43](=[O:44])[CH2:4][CH2:3][C:2]1[CH:1]=[C:47]([C:15]([CH3:18])([CH3:17])[CH3:16])[C:46]([OH:49])=[C:12]([CH3:11])[CH:13]=1)[CH2:10][O:9][C:7](=[O:8])[CH2:6][CH2:5][C:4]1[CH:11]=[C:12]([C:15]([CH3:18])([CH3:17])[CH3:16])[C:13]([OH:14])=[C:2]([CH3:1])[CH:3]=1)[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 176Acetic AcidHCID 165455Methyl 3-(1,1-dimethylethyl)-4-hydroxy-5-methylbenzenepropanoateHCID 2459623-Octadecylsulfanylpropane-1,2-diolHCID 10942334Sodium Methoxide

生成物 1

HCID 21398245HCID 21398245、化合物

反応条件

温度
80 °C

実験手順

A mixture of 15.2 grams (0.06 mole) of methyl 3-methyl-5-tert-butyl-4-hydroxyhydrocinnamate and 10.14 grams (0.027 mole) of 1-n-octadecylthio-2,3-propanediol was heated to about 80° C and stirred until the mixture became homogenous. Sodium methylate (0.292 grams, 0.0054 mole) was added, and the resulting mixture was heated at 125°-145° C for 5 hours at atmospheric pressure and another 3 hours at 135°-145° C at 0.5-5 mm. The reaction mixture was then cooled and the catalyst neutralized with 0.5 grams (0.008 mole) of glacial acetic acid. Purification of the crude product was achieved by first removing the bulk (1.0 g) of the unreacted starting ester under high vacuum in a Hickman molecular still, followed by chromatography from silica gel using benzene as the eluting solvent.

後処理

  1. temperaturethe resulting mixture was heated at 125°-145° C for 5 hours at atmospheric pressure and another 3 hours at 135°-145° C at 0.5-5 mm
  2. temperatureThe reaction mixture was then cooled
  3. customPurification of the crude product
  4. customby first removing the bulk (1.0 g) of the

出典と根拠

ORDレコード
ord-bac46b3b3f004a439a39d6e08104fc3e
出典データセット
uspto-grants-1977_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04058502

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート