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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → HCID 178436709, 화합물

HRID 635266
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HRID 635266 반응식
[CH3:1][O:2][C:3]1[CH:11]=[C:10]([NH2:12])[C:9](S)=[CH:8][C:4]=1[C:5]([OH:7])=O.[Na].C(O[S:18]([O-])(=O)=O)C.Cl.CCO[CH2:26][CH3:27]>O>[CH3:1][O:2][C:3]1[CH:11]=[C:10]([NH2:12])[C:9]([CH2:26][CH3:27])=[CH:8][C:4]=1[C:5]([OH:7])=[S:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 313Hydrochloric AcidHCID 3283Diethyl EtherHCID 34353994-Amino-2-methoxy-5-sulfanylbenzoic acidHCID 3804841Ethyl sulfate anionHCID 5360545Sodium2회

생성물 1

HCID 178436709HCID 178436709, 화합물수율 88%

시약·촉매·용매 1

HCID 962
Water
용매
2회

실험 절차

159 g of 2-methoxy-4-amino-5-mercaptobenzoic acid, 355 cm3 of water and 160 cm3 of 30% sodium hydroxyde solution are placed in a flask fitted with a condenser. The mixture is heated until the solid dissolves, then 123 g of ethylsulfate is added. The mixture is heated to reflux, treated with 10 cm3 of 30% sodium hydroxyde solution, then heated to reflux for 1 hour. After cooling, 800 cm3 of water is added and the solution is filtered. The precipitate obtained by adding 100 cm3 of concentrated hydrochloric acid in the presence of ether is drained, washed with water and dried. 162 g of 2-methoxy-4-amino-5-ethylthio benzoic acid is obtained (yield=88%).

후처리

  1. customfitted with a condenser
  2. temperatureThe mixture is heated until the solid
  3. dissolutiondissolves
  4. temperatureThe mixture is heated
  5. temperatureto reflux
  6. temperatureheated
  7. temperatureto reflux for 1 hour
  8. temperatureAfter cooling
  9. filtrationthe solution is filtered
  10. customThe precipitate obtained
  11. washwashed with water
  12. customdried

출처 및 근거

ORD 기록
ord-e004ecc170f2474cbd6008843b8206aa
출처 데이터셋
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06187807B1

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