HuagongsheHuagongshe Chemistry Print Report · For research reference only
(o-Carboxyphenylthio)acetic acid → 3-Chloro-1-benzothiophene-2-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (o-Carboxyphenylthio)acetic acid | HCID 8660 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Chloro-N,N-dimethylformiminium chloride | HCID 77311 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Chloro-N,N-dimethylformiminium chloride | HCID 77311 | — |
| Product | 3-Chloro-1-benzothiophene-2-carbaldehyde | HCID 818121 | 68% |
Reaction Steps
Vilsmeier reagent was prepared via the dropwise addition of POCl3 (7.9 mL, 84 mmol) into ice-cold DMF (14 mL). A solution of 2-carboxymethylsulfanyl-benzoic acid (3.0 g, 14 mmol) in DMF (15 mL) was added dropwise to the Vilsmeier reagent. The resulting mixture was warmed to room temperature and then heated to 80° C. for 3.5 h. The reaction mixture was cooled to ambient temperature. Crushed ice was added until a bright yellow precipitate appeared. The solid was isolated by filtration. Purification by flash column chromatography (silica gel, hexanes/ethyl acetate 3:2) gave the title compound (1.87 g, 68%) as a yellow powder: 1H NMR (300 MHz, CDCl3) δ 10.36 (s, 1H), 8.03 (m, 1H), 7.86 (m, 1H), 7.59-7.53 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879872B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-c6ebb43eecd24317a3331641aa9a3d91 |
| Source note | uspto-grants-2011_02 |