Thionyl Chloride → HCID 86734598, compound
Reaction equation
[N:1]1([C:6]2[CH:11]=[CH:10][C:9]([CH2:12][C:13]([OH:15])=O)=[CH:8][CH:7]=2)[CH2:5][CH2:4][N:3]=[CH:2]1.S(Cl)([Cl:18])=O>C1C=CC=CC=1>[ClH:18].[N:1]1([C:6]2[CH:11]=[CH:10][C:9]([CH2:12][C:13]([Cl:18])=[O:15])=[CH:8][CH:7]=2)[CH2:5][CH2:4][N:3]=[CH:2]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
10 g of 4-(2-Imidazolinyl)-phenylacetic acid were stirred for 5 hours at 55° C with a mixture of 150 ml of benzene and 90 ml of thionyl chloride. The reaction mixture was then cooled, filtered with suction, washed with benzene and diethyl ether and dried under reduced pressure. 11 g of 4-(2-Imidazolinyl)-phenylacetic acid chloride-hydrochloride were obtained.
Workup
- temperatureThe reaction mixture was then cooled
- filtrationfiltered with suction
- washwashed with benzene and diethyl ether
- customdried under reduced pressure
Sources & evidence
- ORD record
- ord-be4d8f1d817e4afea11c3912ffe557ed
- Source dataset
- uspto-grants-1977_04
- Patent number
- US04018933
Reaction notes
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