Hydrochloric Acid → HCID 13869731, compound
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1[N:7]([CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[C:8]2[C:13]([CH:14]=1)=[CH:12][CH:11]=[CH:10][CH:9]=2)=[O:5])[CH3:2].[ClH:22]>CCOCC>[ClH:22].[CH2:1]([O:3][C:4]([CH:6]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[N:7]1[CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[O:5])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Ethyl-1-benzylindole carboxylate is reduced as in the above example 3. The obtained oil is dissolved in ether and ethanolic hydrogen chloride is added to yield ethyl-1-benzyl-2,3-dihydroindole-carboxylate hydrochloride, m.p. 123°-124° C.
Sources & evidence
- ORD record
- ord-dc2cb3d396474893be6d055a28c516d4
- Source dataset
- uspto-grants-1990_03
- Patent number
- US04912125
Reaction notes
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