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Water → 4-chloro-7-fluoro-1H-indole-2-carboxylic acid ethyl ester

HRID 853064
Notes
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Reaction equation

HRID 853064 reaction equation
C(OC(=O)C(=N[NH:8][C:9]1[CH:14]=[C:13]([Cl:15])[CH:12]=[CH:11][C:10]=1[F:16])C)C.[C:18]1(C)C=CC(S(O)(=O)=O)=C[CH:19]=1.O.[C:30](=[O:33])(O)[O-:31].[Na+].[C:35]1(C)C=CC=C[CH:36]=1>>[CH2:35]([O:31][C:30]([C:18]1[NH:8][C:9]2[C:14]([CH:19]=1)=[C:13]([Cl:15])[CH:12]=[CH:11][C:10]=2[F:16])=[O:33])[CH3:36]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 962WaterHCID 1140TolueneHCID 6101p-Toluenesulfonic acidHCID 516892Sodium BicarbonateHCID 865847132-[(5-Chloro-2-fluoro-phenyl)-hydrazono]-propionic acid ethyl ester

Product 1

HCID 694157714-chloro-7-fluoro-1H-indole-2-carboxylic acid ethyl ester
Yield 23%

Procedure

2-[(5-Chloro-2-fluoro-phenyl)-hydrazono]-propionic acid ethyl ester (13.2 g, 51 mmol) was dissolved in toluene, p-toluenesulfonic acid (10 g, 51 mmol) was added and the mixture was heated to reflux for 24 h with separation of water. The mixture was cooled, neutralized with saturated sodium bicarbonate (400 mL) and extracted thrice with ethyl acetate. Organic phases were pooled, washed with brine, dried with MgSO4 and the solvent was removed in vacuo. The residue was triturated with hexane to yield the title product as yellowish solid (2.9 g, 23%); EI-MS: m/e=241.1 (M+).

Workup

  1. temperaturethe mixture was heated
  2. temperatureThe mixture was cooled
  3. extractionextracted thrice with ethyl acetate
  4. washwashed with brine
  5. dry with materialdried with MgSO4
  6. customthe solvent was removed in vacuo
  7. customThe residue was triturated with hexane

Sources & evidence

ORD record
ord-5199bc7cef8d4b5599e0af3edca56b8d
Source dataset
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07253281B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes