HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexane → HCID 13837943, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Methyl 5-methoxy-1-phenyl-1H-indole-2-carboxylate | HCID 13837942 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 13837943 | HCID 13837943 | 58.9% |
Reaction Steps
A mixture of 4.0 g (0.014 mole) of 5-methoxy-1-phenyl-1H-indole-2-carboxylic acid, methyl ester in 7.0 ml (11.4 g; 0.096 mole) of thionyl chloride (under a nitrogen atmosphere) was stirred at ambient temperature for ten minutes. After the addition of 50 ml of 20% hexane in ether solution, the new mixture was cooled in ice for 30 minutes to precipitate the crude intermediate sulfinyl chloride. The solid was filtered and washed with hexane to yield 3.0 g (63% crude yield) of 3-(chlorosulfinyl)-5-methoxy-1-phenyl-1H-indole-2-carboxylic acid, methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04675332 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-eed663eaa6d644d4bb363f4b50c81f78 |
| Source note | uspto-grants-1987_06 |