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Potassium Hydroxide → HCID 19788163、化合物

HRID 1656480
ノート
印刷プレビュー

反応式

HRID 1656480 の反応式
[OH-].[K+].C[O:4][C:5](=[O:18])[C:6]1[CH:11]=[C:10]([CH3:12])[CH:9]=[C:8]([CH2:13][O:14]C(=O)C)[CH:7]=1>CO.O>[OH:14][CH2:13][C:8]1[CH:7]=[C:6]([CH:11]=[C:10]([CH3:12])[CH:9]=1)[C:5]([OH:18])=[O: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 14797Potassium HydroxideHCID 19788165HCID 19788165、化合物

生成物 1

HCID 19788163HCID 19788163、化合物

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒

反応条件

温度
60 °C

実験手順

In a 5 liter flask were dissolved 380 g (5.77 mole) of 85% KOH in 2.2 liter of methanol and warmed up to 60° C. The methyl-3-acetoxymethyl-5-methylbenzoate from the previous step was added and heated with stirring at 60° C. for 2.5 hrs. The reaction mixture was cooled down to room temperature and the solvent eliminated in the rotavap. The resulting oil was dissolved in 1.5 liter of water and then washed with ethyl ether (1×1 liter). The aqueous layer was made acidic with concentrated hydrochloric acid and the resulting acidic suspension was extracted with ethyl acetate (3×350 ml). The combined organic extracts were then washed with water (2×600 ml) and then brine (2×500 ml), dried over sodium sulfate and concentrated in the rotavap to give 287.6 g of 3-hydroxymethyl-5-methylbenzoic acid.

後処理

  1. temperatureheated
  2. temperatureThe reaction mixture was cooled down to room temperature
  3. washwashed with ethyl ether (1×1 liter)
  4. extractionthe resulting acidic suspension was extracted with ethyl acetate (3×350 ml)
  5. washThe combined organic extracts were then washed with water (2×600 ml)
  6. dry with materialbrine (2×500 ml), dried over sodium sulfate
  7. concentrationconcentrated in the rotavap

出典と根拠

ORDレコード
ord-c046b336c35d4d9f852a7ea97be6d872
出典データセット
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05254584

反応ノート

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