Chlorosuccinimide → 3-Chloro-5-cyano-3-methylthiooxindole
Reaction equation
[C:1]([C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7](=[S:12])[CH:6]2[CH3:13])#[N:2].[Cl:14]N1C(=O)CCC1=O>C(Cl)Cl>[Cl:14][C:6]1([CH3:13])[C:5]2[C:9](=[CH:10][CH:11]=[C:3]([C:1]#[N:2])[CH:4]=2)[NH:8][C:7]1=[S:12]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 5-cyano-3-methylthiooxindole (950 mg, 4.66 mmol) and N-chlorosuccinimide (800 mg, 5.95 mmol) in 100 ml of methylene chloride was stirred at room temperature for 24 hours. The solvent was removed in vacuo, yielding 3-chloro-5-cyano-3-methylthiooxindole and the residue, which was dissolved in a minimum of tetrahydrofuran, was added to a vigorously stirred slurry of red mercuric oxide (1.00 g, 4.7 mmol) and boron trifluoride ethereate (670 mg, 4.7 mmol) in 100 ml of 50 percent aqueous tetrahydrofuran. After 2 hours, the reaction mixture was filtered through a pad of Celite. The pad was washed with three 100-ml portions of chloroform. The organic layer was separated, dried over anhydrous magnesium sulfate, filtered, and the filtrate was evaporated. The residue was chromatographed on silica gel. Elution with chloroform-ethanol (9:1 v/v) gave 5-cyanoisatin as an orange solid (525 mg, 65%), mp 270°-272° (dec); ir (KBr) 3100 (NH), 2220 (C≡N), 1730 (C=O) and 1710 cm-1 (C=O); nmr (DMSO-d6)τ-1.30 (1H, b s, NH), 2.00 (d of d, 1H, J4,6 =2 Hz, J6,7 =8.5 Hz, H6), 2.10 (d, 1H, J4,6 =2 Hz, H4), and 2.90 (d, 1H, J6,7 =8.5 Hz, H7); mass spectrum, m/e obs. 172.0238 (calc. 172.0272).
Workup
- customThe solvent was removed in vacuo
Sources & evidence
- ORD record
- ord-b70d3a061a394c5ebb0415dd170d823e
- Source dataset
- uspto-grants-1980_01
- Patent number
- US04186132
Reaction notes
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