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Methyl Chloride → HCID 53801387、化合物

HRID 918302
ノート
印刷プレビュー

反応式

HRID 918302 の反応式
[CH2:1]([C:8]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)([OH:15])[C:9]([O:11][CH2:12][CH:13]=[CH2:14])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:22]Cl>CN(C)C=O>[CH2:1]([C:8]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)([O:15][CH3:22])[C:9]([O:11][CH2:12][CH:13]=[CH2:14])=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 6327Methyl ChlorideHCID 54410738HCID 54410738、化合物

生成物 1

HCID 53801387HCID 53801387、化合物

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒2 回

実験手順

Into a suspension of 0.75 g of 66% sodium hydride-paraffin in 20 cc of dimethylformamide was added a solution of 5.6 g of allyl α-benzyl-α-hydroxyphenylacetate in 10 cc of dimethylformamide under cooling, and the mixture was stirred for 1 hour. Successively, methyl chloride was introduced into the mixture. The reaction mixture was poured in ice-water and the resultant was subjected to extraction with ether. The ether extract was washed with an aqueous solution saturated with sodium chloride, and dried over sodium sulfate. Thereafter, ether was distilled out and paraffin was removed, whereby, 5.1 g oily allyl α-benzyl-α-methoxyphenylacetate, nD25 1.5488 was obtained.

後処理

  1. temperatureunder cooling
  2. extractionthe resultant was subjected to extraction with ether
  3. extractionThe ether extract
  4. washwas washed with an aqueous solution saturated with sodium chloride
  5. dry with materialdried over sodium sulfate
  6. distillationThereafter, ether was distilled out and paraffin
  7. customwas removed

出典と根拠

ORDレコード
ord-ef9b0cdaeee342b6875e0026eb65d940
出典データセット
uspto-grants-1976_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03970703

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート