HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenyltrimethylammonium bromide dibromide → HCID 22473722, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenyltrimethylammonium bromide dibromide | HCID 17977687 | — |
| Reactant | HCID 22473848 | HCID 22473848 | — |
| Product | HCID 22473722 | HCID 22473722 | 230.4% |
Reaction Steps
In a similar manner to Example 18, methylthioglycolate (13 g) was reacted with 3-chloro-2-fluorobenzaldehyde (19.57 g) in dimethylformamide to give methyl 7-chlorobenzo[b]thiophene-2-carboxylate, which was hydrolysed, chlorinated and reacted with N,O-dimethylhydroxylamine hydrochloride to give 7-chloro-N-methoxy-N-methylbenzo[b]thiophene-2-carboxamide, which was reacted with ethylmagnesium bromide to give 1-(7-chlorobenzo[b]thiophen-2-yl)propan-1-one. This ketone (1.17 g) was reacted with phenyltrimethylammonium tribromide (2.15 g) to give 2-bromo-1-(7-chlorobenzo[b]thiophen-2-yl)propan-1-one (2.32 g) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06900216B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-dce7380ed39c4a349b587914d2adadf4 |
| Source note | uspto-grants-2005_05 |