HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

3-(3,4-Dichlorophenyl)propionic acid → 5,6-Dichloro-2,3-dihydro-1H-inden-1-one

HRID 1648207
Notes
Print preview

Reaction equation

HRID 1648207 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:9][CH2:10][C:11]([OH:13])=O)[CH:5]=[CH:6][C:7]=1[Cl:8]>S(Cl)(Cl)=O>[Cl:1][C:2]1[CH:3]=[C:4]2[C:5](=[CH:6][C:7]=1[Cl:8])[C:11](=[O:13])[CH2:10][CH2:9]2
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 1411813-(3,4-Dichlorophenyl)propionic acid

Product 1

HCID 229036095,6-Dichloro-2,3-dihydro-1H-inden-1-one

Reagents, catalysts & solvents 1

HCID 24386Thionyl ChlorideSolvent

Conditions

Temperature
50 °C

Procedure

A mixture of 20 g of 3-(3,4-dichlorophenyl)-propionic acid [J. Med. Chem., Vol. 16(2) (1973), p. 101-106] and 100 ml of thionyl chloride was refluxed for 30 minutes and the thionyl chloride was then evaporated. The residue was taken up in 20 ml of methylene chloride and the solution was poured into a suspension of 20 g of aluminum chloride in 150 ml of methylene chloride. The mixture was stirred for one hour at room temperature and 30 minutes at 50° C. The mixture was poured over ice and was stirred for 30 minutes and then was extracted with methylene chloride.

Workup

  1. temperaturewas refluxed for 30 minutes
  2. customthe thionyl chloride was then evaporated
  3. additionthe solution was poured into a suspension of 20 g of aluminum chloride in 150 ml of methylene chloride
  4. additionThe mixture was poured over ice
  5. stirringwas stirred for 30 minutes
  6. extractionwas extracted with methylene chloride

Sources & evidence

ORD record
ord-7b5fe474e06f46448b42d582990bfb06
Source dataset
uspto-grants-1995_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05436244

Reaction notes

Loading…

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes