Hydrochloric Acid → HCID 12929145, compound
Reaction equation
[CH3:1][S:2]([CH:5]1[C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=2[CH2:9][O:8][C:7]2[CH:16]=[CH:17][C:18]([C:20]([O:22]C)=[O:21])=[CH:19][C:6]1=2)(=[O:4])=[O:3].[OH-].[Na+].Cl>O>[CH3:1][S:2]([CH:5]1[C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=2[CH2:9][O:8][C:7]2[CH:16]=[CH:17][C:18]([C:20]([OH:22])=[O:21])=[CH:19][C:6]1=2)(=[O:4])=[O:3]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Reflux 1 gm. of the ester of Step A and 40 cc. of 1 N aqueous sodium hydroxide for 15 minutes. Strip to dryness and dissolve the residue in water. Acidify with aqueous hydrochloric acid. Separate the solids by filtration to obtain the title product (m.p. 251° C. dec.).
Workup
- temperatureReflux 1 gm
- customSeparate the solids
- filtrationby filtration
Sources & evidence
- ORD record
- ord-f95130f624694dc18cad3d9e7606e10a
- Source dataset
- uspto-grants-1981_08
- Patent number
- US04282365
Reaction notes
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