Acetic Anhydride → HCID 86738690, compound
Reaction equation
[N+]([C:4]1[CH:14]=[C:13]([N+:15]([O-:17])=[O:16])[CH:12]=[C:6]2[C:7]([O:9][C:10](=O)[C:5]=12)=[O:8])([O-])=O.C1([SH:24])C=CC=CC=1.C(O[C:29](=O)[CH3:30])(=O)C.[OH-].[Na+].O1[CH2:38][CH2:37][CH2:36][CH2:35]1>[Cl-].C([N+](CC)(CC)CC)C1C=CC=CC=1.C(Cl)Cl>[N+:15]([C:13]1[C:12]([C:30]2[CH:29]=[CH:38][CH:37]=[CH:36][CH:35]=2)=[C:6]2[C:7](=[O:8])[O:9][C:10](=[S:24])[C:5]2=[CH:4][CH:14]=1)([O-:17])=[O:16]Participants
8
Procedure
5 g (21 mmols) of 3,5-dinitrophthalic anhydride are dissolved in 17 ml of tetrahydrofuran; 2.78 g (25.2 mmols) of thiophenol and 4.3 g (42 mmols) of acetic anhydride are then added. This solution is added dropwise, with vigorous stirring, to a mixture of 22.4 g of 30% sodium hydroxide solution, 47.8 mg (0.21 mmol) of benzyltriethylammonium chloride and 100 ml of methylene chloride.
Sources & evidence
- ORD record
- ord-a476717ad34e4e3286d8c405c10d441a
- Source dataset
- uspto-grants-1982_12
- Patent number
- US04363917
Reaction notes
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