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Sodium Methoxide → HCID 53801387、化合物

HRID 918303
ノート
印刷プレビュー

反応式

HRID 918303 の反応式
[CH3:1][O-:2].[Na+].[CH2:4]([C:11]([C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)(Cl)[C:12]([O:14][CH2:15][CH:16]=[CH2:17])=[O:13])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1>CO>[CH2:4]([C:11]([C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)([O:2][CH3:1])[C:12]([O:14][CH2:15][CH:16]=[CH2:17])=[O:13])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=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 10942334Sodium MethoxideHCID 54032347HCID 54032347、化合物

生成物 1

HCID 53801387HCID 53801387、化合物収率 94.7%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

Into a solution of 1.1 g of sodium methylate in 20 cc of methanol was added a solution of 6.0 g of allyl α-benzyl-α-chlorophenylacetate in 10 cc of methanol under cooling, and the mixture was stirred for 2 hours, whereby white precipitates were deposited. The reaction mixture was poured in 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, and thereafter evaporation of ether gave 5.6 g of oily allyl α-benzyl-α-methoxyphenylacetate, nD25 1.5486.

後処理

  1. temperatureunder cooling
  2. customwhereby white precipitates
  3. additionThe reaction mixture was poured in water
  4. extractionthe resultant was subjected to extraction with ether
  5. extractionThe ether extract
  6. washwas washed with an aqueous solution saturated with sodium chloride
  7. dry with materialdried over sodium sulfate
  8. customevaporation of ether

出典と根拠

ORDレコード
ord-3329db3e4bf54be7b7590c75522dc97e
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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