Ammonium Chloride → HCID 15341803、化合物

HRID 1033631ノート

反応式

HRID 1033631 の反応式
[OH:1][C:2]1[C:11]([CH2:12][CH:13]=[CH2:14])=[C:10]([OH:15])[CH:9]=[CH:8][C:3]=1[C:4](OC)=[O:5].[Cl-].[NH4+:17]>C(O)C>[OH:1][C:2]1[C:11]([CH2:12][CH:13]=[CH2:14])=[C:10]([OH:15])[CH:9]=[CH:8][C:3]=1[C:4]([NH2:17])=[O:5]

参加物

4

反応物 2

HCID 25517Ammonium ChlorideHCID 13019279Methyl 2,4-dihydroxy-3-(prop-2-en-1-yl)benzoate

生成物 1

HCID 15341803HCID 15341803、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
50 °C

実験手順

Methyl 2,4-dihydroxy-3-(2-propenyl)benzoate (4.4 g) was added to a mixture of about 10 to 15 ml of saturated ammonium chloride solution and 2 to 3 ml of ethanol. The reaction mixture was stirred overnight at 50° C. The reaction mixture was extracted five times with ethyl acetate, and the organic layer was concentrated under vacuum. The product was crystallized and recrystallized from chloroform. Subsequent chromatography of the precipitated product on a 25 g silica gel column with 40% ethyl acetate/hexane as eluant gave the pure product.

後処理

  1. extractionThe reaction mixture was extracted five times with ethyl acetate
  2. concentrationthe organic layer was concentrated under vacuum
  3. customThe product was crystallized
  4. customrecrystallized from chloroform
  5. customSubsequent chromatography of the precipitated product on a 25 g silica gel column with 40% ethyl acetate/hexane as eluant gave the pure product

出典と根拠

ORDレコード
ord-474898591a7246b684160e620283ef73
出典データセット
uspto-grants-1994_05
特許番号
US05310951

反応ノート

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