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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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3-(2-aminoethyl)benzoic acid → Benzoic Acid

HRID 2051606
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반응식

HRID 2051606 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 5060773-(2-aminoethyl)benzoic acidHCID 517045Sodium AcetateHCID 54192812HCID 54192812, 화합물

생성물 1

HCID 243Benzoic Acid

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-e09a6bed016e41418d602499804ea3f8
출처 데이터셋
uspto-grants-1980_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04181658

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