HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Anisoyl chloride → HCID 10808337, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | 2-Benzyl-1-benzothiophene | HCID 12758157 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Product | HCID 10808337 | HCID 10808337 | 85% |
Reaction Steps
The known compound, 2-benzyl-benzo[b]thiophene (CA reg. no. 3407-15-6) was acylated with one equilvalent of anisoyl chloride using one equivalent of a tin (IV) chloride promoter in carbon disulfide solvent to afford (2-benzyl-benzo[b]thiophen-3-yl)-(4-methoxy-phenyl)-methanone (85% yield). This compound was demethylated using six equivalents of pyridinium hydrocholide at 228° C. to afford (2-benzyl-benzo[b]thiophen-3-yl)-(4-hydroxy-phenyl)-methanone (90% yield). This compound was brominated according to the procedure in Example 4 to afford the tide compound as a white solid (95% yield): mp 155.5-156.5; MS m/e 500 (M)+;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06844358B2 |
| Source dataset | uspto-grants-2005_01 |
| ORD ID | ord-b6e951cd034a4f71bbe30a9643e1fb28 |
| Source note | uspto-grants-2005_01 |