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Sodium Hydroxide → 3-[4-(Hydroxymethyl)phenyl]propanoic acid

HRID 1287360
ノート
印刷プレビュー

反応式

HRID 1287360 の反応式
Cl[CH2:2][C:3]1[CH:13]=[CH:12][C:6]([CH2:7][CH2:8][C:9]([OH:11])=[O:10])=[CH:5][CH:4]=1.[OH-].[Na+].C1C=C(C(C2C=CC(O)=CC=2)C2C=CC([OH:29])=CC=2)C(C(O)=O)=CC=1>O>[OH:29][CH2:2][C:3]1[CH:13]=[CH:12][C:6]([CH2:7][CH2:8][C:9]([OH:11])=[O:10])=[CH:5][CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 14798Sodium Hydroxide2 回HCID 66494PhenolphthalinHCID 2032212856703-33-4

生成物 1

HCID 203221243-[4-(Hydroxymethyl)phenyl]propanoic acid

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

30 g (0.15 mol) of 4-chloromethyl-hydrocinnamic acid (J.Org, Chem. 26, 148 (1961) in 200 ml of water were neutralized with a 10% sodium hydroxide solution against phenol phthaline. 10% of NaOH (on the whole about 60 ml) were added dropwise, while stirring at reflux temperature, to the solution obtained in the same measure as it was consumed. When the reaction was finished, the mixture was saturated with sodium chloride, acidifed with concentrated hydrochloric acid, the product precipitated was suction-filtered and washed with water. Melting point: 124° - 126°C.

後処理

  1. temperatureat reflux temperature
  2. customto the solution obtained in the same measure as it
  3. customwas consumed
  4. customthe product precipitated
  5. filtrationwas suction-filtered
  6. washwashed with water

出典と根拠

ORDレコード
ord-4f89c3a9a09b4d698e8d22c5e6223522
出典データセット
uspto-grants-1976_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03984459

反応ノート

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