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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 4-Azidobenzoic acid

HRID 358227
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HRID 358227 반응식
[NH2:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1.Cl.N([O-])=O.[Na+].[N-:16]=[N+:17]=[N-].[Na+]>O>[N:1]([C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1)=[N+:16]=[N-:17]
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 9784-Aminobenzoic AcidHCID 33557Sodium AzideHCID 23668193Sodium Nitrite

생성물 1

HCID 30341844-Azidobenzoic acid

시약·촉매·용매 1

HCID 962Water용매3회

실험 절차

13.7 g of p-aminobenzoic acid was dispersed in a solution of 100 cc of water and 30 cc of 30% hydrochloric acid in an ordinary manner and the dispersion was cooled with ice. A solution of 8.3 g of sodium nitrite in 50 cc of water was added dropwise to the dispersion to effect the diazotization reaction. A solution of 10.1 g of sodium azide in 70 cc of water was added dropwise to the mixture, stirred for about one hour, filtered and vacuum-dried to obtain p-azidobenzoic acid. 5.4 g of the thus obtained p-azidobenzoic acid was dissolved in 10 cc of dimethylformamide and 25 g of thionyl chloride was added dropwise to the solution. The mixture was stirred for about one hour and the product was added dropwise to ice-water. After filtration followed by washing with water and vacuum drying, p-azidobenzoyl chloride was obtained.

후처리

  1. temperaturethe dispersion was cooled with ice
  2. customthe diazotization reaction
  3. filtrationfiltered
  4. customvacuum-dried

출처 및 근거

ORD 기록
ord-0b27ffc5dd0c4205b822984128c69f0e
출처 데이터셋
uspto-grants-1984_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04465768

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