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Hydrochloric Acid → 1-(3-Acetylthiopropanoyl)-3,3-dimethylindoline-2-carboxylic acid

HRID 745606
Notes
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Reaction equation

HRID 745606 reaction equation
C(N(CC)CC)C.Cl.[CH3:9][C:10]1([CH3:22])[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[NH:12][CH:11]1[C:19]([OH:21])=[O:20].[C:23]([S:26][CH2:27][CH2:28][C:29](Cl)=[O:30])(=[O:25])[CH3:24].Cl>C(Cl)Cl>[C:23]([S:26][CH2:27][CH2:28][C:29]([N:12]1[C:13]2[C:18](=[CH:17][CH:16]=[CH:15][CH:14]=2)[C:10]([CH3:22])([CH3:9])[CH:11]1[C:19]([OH:21])=[O:20])=[O:30])(=[O:25])[CH3:24]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 8471TriethylamineHCID 129431223-(Acetylsulfanyl)propanoyl chlorideHCID 704701543,3-dimethyl-2,3-dihydro-1H-indole-2-carboxylic acid hydrochloride

Product 1

HCID 233138381-(3-Acetylthiopropanoyl)-3,3-dimethylindoline-2-carboxylic acid

Reagents, catalysts & solvents 1

HCID 6344
Dichloromethane
Solvent
2×

Procedure

0.93 g of triethylamine are added to the suspension of 0.7 g of 3,3-dimethylindoline-2-carboxylic acid hydrochloride in 20 ml of methylene chloride and the resulting solution is cooled to -10°. The solution of 0.51 g of 3-acetylthiopropanoyl chloride in 5 ml of methylene chloride is added dropwise and the mixture stirred at -5° to -10° for 1 hour and at room temperature for 3 hours. It is cooled to 0° and treated with 10 ml of 3N hydrochloric acid. The organic layer is separated and the aqueous solution further extracted with methylene chloride. The combined methylene chloride solutions are dried and evaporated, to give the 1-(3-acetylthiopropanoyl)-3,3-dimethylindoline-2-carboxylic acid as a foam.

Workup

  1. temperaturethe resulting solution is cooled to -10°
  2. temperatureIt is cooled to 0°
  3. customThe organic layer is separated
  4. extractionthe aqueous solution further extracted with methylene chloride
  5. dry with materialThe combined methylene chloride solutions are dried
  6. customevaporated

Sources & evidence

ORD record
ord-fb23bb495720428daa47716788fc5e74
Source dataset
uspto-grants-1986_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04599357

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes