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3-(2-aminoethyl)benzoic acid → Benzoic Acid

HRID 2051606
ノート
印刷プレビュー

反応式

HRID 2051606 の反応式
NCC[C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][CH:12]=1)[C:7]([OH:9])=[O:8].C([O-])(=O)C.[Na+].C(N1C=CC=C(C(Cl)=O)C1=O)C1C=CC=CC=1>CC(C)=O>[C:7]([OH:9])(=[O:8])[C:6]1[CH:10]=[CH:11][CH:12]=[CH:4][CH:5]=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 5060773-(2-aminoethyl)benzoic acidHCID 517045Sodium AcetateHCID 54192812HCID 54192812、化合物

生成物 1

HCID 243Benzoic Acid

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

20 ml of acetone are added to 16 ml of an about 1 molar solution of 3-(2-aminoethyl)-benzoic acid containing the corresponding amount of sodium acetate, and 3.7 g of 1-benzyl-1,2-dihydro-2-oxo-nicotinic acid chloride (prepared from 1-benzyl-1,2-dihydro-2-oxo-nicotinic acid and thionyl chloride) are added with agitation and cooling. Agitation is then continued for 1 hour at room temperature, the acetone is removed under reduced pressure, and dilute hydrochloric acid is added to the residue. The precipitated product is suction-filtered, reprecipitated from dilute ammonia, and recrystallized from dilute methanol. The 4-(2-<1-benzyl-1,2-dihydro-2-oxo-nicotinamido>-ethyl)-benzoic acid so obtained has a melting point of 150°-152° C. and of 171°-173° C.

後処理

  1. additionare added with agitation
  2. temperaturecooling
  3. customthe acetone is removed under reduced pressure, and dilute hydrochloric acid
  4. additionis added to the residue
  5. filtrationThe precipitated product is suction-filtered
  6. customreprecipitated from dilute ammonia
  7. customrecrystallized from dilute methanol

出典と根拠

ORDレコード
ord-e09a6bed016e41418d602499804ea3f8
出典データセット
uspto-grants-1980_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04181658

反応ノート

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