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Ethanolamine → 2-Amino-5-(4-[2-hydroxyethyl]aminophenylsulfonyloxy)nitrobenzene

HRID 1823761
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HRID 1823761 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][S:9]([C:12]2[CH:17]=[CH:16][C:15](F)=[CH:14][CH:13]=2)(=[O:11])=[O:10])=[CH:4][C:3]=1[N+:19]([O-:21])=[O:20].[CH2:22]([CH2:24][NH2:25])[OH:23]>CCOCCO.Cl>[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][S:9]([C:12]2[CH:17]=[CH:16][C:15]([NH:25][CH2:24][CH2:22][OH:23])=[CH:14][CH:13]=2)(=[O:11])=[O:10])=[CH:4][C:3]=1[N+:19]([O-:21])=[O:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 700EthanolamineHCID 120188434-Amino-3-nitrophenyl 4-fluorobenzenesulfonate

생성물 1

HCID 120188442-Amino-5-(4-[2-hydroxyethyl]aminophenylsulfonyloxy)nitrobenzene

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 8076Glycol monoethyl ether용매

실험 절차

15.6 g of 2-amino-5-(4-fluorophenylsulfonyloxy)nitrobenzene were combined with 25 ml ethanolamine in 100 ml ethyl glycol in a round bottom flask. The reaction mixture was heated to reflux for 90 min and then cooled on ice. Reaction mixture was then diluted with 250 ml of 2N aqueous HCl, the compound precipitated and was filtered off with suction. The preciptate was the washed with water and dried, yielding 15.5 g of 2-amino-5-(4-[2-hydroxyethyl]aminophenylsulfonyloxy)nitrobenzene (melting point 180° C.).

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux for 90 min
  3. temperaturecooled on ice
  4. customReaction mixture
  5. customthe compound precipitated
  6. filtrationwas filtered off with suction
  7. washwashed with water
  8. customdried

출처 및 근거

ORD 기록
ord-04eeb12c40554426b59a777a8d6f45d5
출처 데이터셋
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07041668B2

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