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Diethylamine → 4-((Diethylamino)methyl)benzoic acid hydrochloride

HRID 1600817
ノート
印刷プレビュー

反応式

HRID 1600817 の反応式
[Cl:1][CH2:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=[O:8])=[CH:5][CH:4]=1.[CH2:12]([NH:14][CH2:15][CH3:16])[CH3:13]>C(O)C.[OH-].[Na+]>[ClH:1].[CH2:12]([N:14]([CH2:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=[O:8])=[CH:5][CH:4]=1)[CH2:15][CH3:16])[CH3:13]
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 2

HCID 8021DiethylamineHCID 742344-(Chloromethyl)benzoic acid

生成物 1

HCID 122990074-((Diethylamino)methyl)benzoic acid hydrochloride収率 55.6%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 14798Sodium Hydroxide溶媒

実験手順

To a solution of 4-chloromethylbenzoic acid (17.1 g, 0.1 mol) in ethanol (200 ml) cooled in an ice bath was added dropwise diethylamine (32.2 g, 0.44 mol) over 20 minutes. The reaction mixture was refluxed for 17 hours, cooled to room temperature and the solvent was stripped. The residue was dissolved in 1N NaOH (50 ml), extracted with ether (50-100 ml) and the aqueous layer was acidified with 2N HCl to a pH of 3. The aqueous layer was stripped and the residue was treated with ethanol, filtered and the ethanol was stripped. The residue was recrystallized from isopropyl alcohol (3×) to afford 13.54 g of 4-diethylaminomethyl benzoic acid hydrochloride, m.p. 189-191° C.

後処理

  1. temperatureThe reaction mixture was refluxed for 17 hours
  2. extractionextracted with ether (50-100 ml)
  3. additionthe residue was treated with ethanol
  4. filtrationfiltered
  5. customThe residue was recrystallized from isopropyl alcohol (3×)

出典と根拠

ORDレコード
ord-a90bcb4f00504f04ab44868373898af6
出典データセット
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05977118

反応ノート

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