HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde, 4-hexyl- → HCID 18435227, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde, 4-hexyl- | HCID 170813 | — |
| Reactant | 2-Amino-3,4-difluorobenzene-1-thiol | HCID 18435226 | — |
| Product | HCID 18435227 | HCID 18435227 | — |
Reaction Steps
2-Amino-3,4-difluorothiophenol [131105-92-5] is reacted analogously to Reference 1 with 4-hexylbenzaldehyde (commercially available, [49763-69-1]) to give 4,5-difluoro-2-(4-hexylphenyl)benzothiazoline, which is converted into 4,5-difluoro-2-(4-hexylphenyl)benzothiazole using barium permanganate by the method described in the cited literature. a-Lithiation (by means of lithium diisopropylamide analogously to J. Chem. Soc. Perkin Trans. II 1989, 2048) and quenching with hexyl bromide gives the target compound, which can be purified by chromatography and by recrystallization from acetonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06436489B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-3475607acc5d4e5ba6e4d17fb30b336b |
| Source note | uspto-grants-2002_08 |