HuagongsheHuagongshe Chemistry Print Report · For research reference only
Stannous chloride dihydrate → 6-bromo-7-chloro-3,4-dihydroquinoxalin-2(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | HCID 21189956 | HCID 21189956 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-bromo-7-chloro-3,4-dihydroquinoxalin-2(1H)-one | HCID 10038316 | 86% |
Reaction Steps
A solution of N-(5'-bromo-4'-chloro-2'-nitrophenyl)glycine sodium salt (0.255 g, 0.824 mmol, as prepared above) and tin (II) chloride dihydrate (0.560 g, 2.48 mmol, Aldrich, used as received) in ethanol (6 mL) was refluxed for 3 h. It was then cooled to room temperature and allowed to stand overnight at room temperature. The white solid was filtered and dried to yield 0.038 g (18%) of the pure (1H NMR) title compound as white flakes; m.p. 230-232° C.; 1H NMR (DMSO-d6): δ 3.732 (s, 2H), 6.371 (s, 1H), 6.830 (s, 1H), 6.912 (s, 1H), 10.437 (s, 1H). Extraction of the filtrate with ethyl acetate (30 mL) gave 0.136 g (68%) more product for a combined yield of 86%. The product was used as such for the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05977107 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-d286d5b1cbdc4966a03563c0c4813ddc |
| Source note | uspto-grants-1999_11 |