HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Xylene → HCID 54536413, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Ethyl 6-cyanohexanoate | HCID 24976 | — |
| Reactant | Benzenethiol, 2-amino-3,4,6-trifluoro-, hydrochloride | HCID 11390282 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 54536413 | HCID 54536413 | 40% |
Reaction Steps
To xylene (6 ml) was added 2-amino-3,4,6-trifluorothiophenol hydrochloride (647 mg, 3 mmol), 6-cyanohexanoic acid ethyl ester (507 mg, 3 mmol) and ethanol (0.5 ml) and the mixture was heated to reflux for 60 hours under a nitrogen stream. The resultant reaction mixture was washed with water, dried and then evaporated to yield a residue, which was purified on a silica gel column to give 6-(4,5,7-trifluorobenzothiazol-2-yl)hexanoic acid ethyl ester (395 mg, 40%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05700819 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-a641376a0374424086cbe4cf57ea4219 |
| Source note | uspto-grants-1997_12 |