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4-Methoxybenzalcyanoacetic acid → 2-Cyano-3-(4-methoxyphenyl)propanoic acid

HRID 980794
ノート
印刷プレビュー

反応式

HRID 980794 の反応式
[BH4-].[Na+].[C:3]([C:5](=[CH:9][C:10]1[CH:15]=[CH:14][C:13]([O:16][CH3:17])=[CH:12][CH:11]=1)[C:6]([OH:8])=[O:7])#[N:4]>C([O-])(O)=O.[Na+].CO>[C:3]([CH:5]([CH2:9][C:10]1[CH:11]=[CH:12][C:13]([O:16][CH3:17])=[CH:14][CH:15]=1)[C:6]([OH:8])=[O:7])#[N:4]
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 2

HCID 2332604-Methoxybenzalcyanoacetic acidHCID 4311764Sodium borohydride

生成物 1

HCID 137111482-Cyano-3-(4-methoxyphenyl)propanoic acid

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 516892Sodium Bicarbonate溶媒

反応条件

温度
15 °C

実験手順

Sodium borohydride (30.2 g) is added portionwise over a period of 2 hours to a stirred mixture of α-cyano-4-methoxycinnamic acid (52.5 g) in aqueous saturated NaHCO3 (200 ml) and methanol (600 ml) cooled to about 15° C. The reaction mixture is allowed to warm to RT, stirred at RT for 30 min and concentrated in vacuo. The residue is partitioned between water and ether and the aqueous layer acidified and extracted with ether. The ether extract is washed, dried over Na2SO4, filtered and the filtrate evaporated in vacuo producing a liquid which is crystallized from toluene yielding the desired product as a solid, M.P. 94°-95° C.

後処理

  1. temperatureto warm to RT
  2. concentrationconcentrated in vacuo
  3. customThe residue is partitioned between water and ether
  4. extractionextracted with ether
  5. extractionThe ether extract
  6. washis washed
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. customthe filtrate evaporated in vacuo
  10. customproducing a liquid which
  11. customis crystallized from toluene yielding the desired product as a solid, M.P. 94°-95° C.

出典と根拠

ORDレコード
ord-2ebf1a6f27a740fdad2214f3df4107a4
出典データセット
uspto-grants-1987_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04639442

反応ノート

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