Hydrochloric Acid → HCID 57235519, compound
Reaction equation
[Cl:1][C:2]1[CH:31]=[CH:30][C:5]([C:6]([N:8]2[C:16]3[C:11](=[CH:12][C:13]([O:17][CH3:18])=[CH:14][CH:15]=3)[C:10]([C:19](=[N:21][O:22]C3CCCCO3)[CH3:20])=[C:9]2[CH3:29])=[O:7])=[CH:4][CH:3]=1.Cl.[OH-].[NH4+]>O1CCCC1>[Cl:1][C:2]1[CH:31]=[CH:30][C:5]([C:6]([N:8]2[C:16]3[C:11](=[CH:12][C:13]([O:17][CH3:18])=[CH:14][CH:15]=3)[C:10]([C:19](=[N:21][OH:22])[CH3:20])=[C:9]2[CH3:29])=[O:7])=[CH:4][CH:3]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 1-(4-chlorobenzoyl)-5-methoxy-2-methyl -3-[1-[[(tetrahydro-2H-pyran-2-yl)oxy]imino]ethyl]-lH-indole (5.0 g, 11.3 mmol) in tetrahydrofuran (115 ml) is added 10 ml of concentrated hydrochloric acid. The reaction mixture is stirred for 21/2 hours, at which time it is neutralized with concentrated ammonium hydroxide. It is concentrated to near dryness, diluted with ethyl acetate and washed twice with water and once with a saturated solution of sodium chloride. The organic phase is further dried over magnesium sulfate, filtered, and concentrated slowly in vacuo to 50 ml. The powdery crystals are collected to give 2.8 g (70.4%) of pure 1-(4-chlorobenzoyl)-3-[1-(hydroxyimino)ethyl]-5-methoxy-2-methyl-lH-indole; mp darkens (chars) at 170°-197° C. (dec).
Workup
- concentrationIt is concentrated
- additiondiluted with ethyl acetate
- washwashed twice with water and once with a saturated solution of sodium chloride
- dry with materialThe organic phase is further dried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated slowly in vacuo to 50 ml
- customThe powdery crystals are collected
Sources & evidence
- ORD record
- ord-5418a4b596b141e5ad03658dabb5d6bb
- Source dataset
- uspto-grants-1991_12
- Patent number
- US05075330
Reaction notes
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