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

HRID 2083112
ノート
印刷プレビュー

反応式

HRID 2083112 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, acidified 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-67ffe46d7bdb4acb84887d3a0e03fa94
出典データセット
uspto-grants-1978_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04083990

反応ノート

読み込み中…

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