HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Fluoro-6-methylthioindole-2,3-dione → 5-Fluoro-6-methylthioindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Fluoro-6-methylthioindole-2,3-dione | HCID 22612730 | — |
| Reactant | 7-chloro-5-fluoro-1H-indole | HCID 22612740 | — |
| Product | 5-Fluoro-6-methylthioindole | HCID 22612702 | — |
Reaction Steps
5-Fluoro-6-methylthioindole was prepared from 5-fluoro-6-methylthioindole-2,3-dione according to the method described in the preparation of 7-chloro-5-fluoroindole as a white solid (1.21 g, 37%): mp 51° C.; C9H8FNS requires: C, 59.65; H, 4.45; N, 7.73; S, 17.69%. Found C, 59.75; H, 4.44; N, 7.72; S, 17.65%; IR δmax (Nujol)/cm−1 3461, 3408, 3361, 2925, 2855, 1455, 1304 and 1137; NMR δH (400 MHz, CDCl3) 2.49 (3H, s), 6.49-6.51 (1H, m), 7.22 (1H, t, J 3.0 Hz), 7.30 (1H, d, J 10.0 Hz), 7.36 (1H, d, J 6.5 Hz), 8.0-8.25 (1H, brm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06380238B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-86c99572b5df4a499b5d4e78c17118ce |
| Source note | uspto-grants-2002_04 |