HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-[[2-(1-Methylethyl)-3-indolizinyl]sulfonyl]phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 14555118 | HCID 14555118 | — |
| Solvent | Ethanethiol | HCID 6343 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[[2-(1-Methylethyl)-3-indolizinyl]sulfonyl]phenol | HCID 10335851 | — |
Reaction Steps
6.7 g (0.050 mole) of aluminium chloride are suspended in 100 ml of dichloromethane and 25 ml of ethanethiol. This suspension is stirred and cooled to 0° C. while 2.5 g of 2-isopropyl 3-p-methoxyphenylsulfonyl indolizine in dichloromethane are added. The addition takes about 15 minutes. The reaction mixture is allowed to warm to room temperature and maintained there for 45 minutes. It is poured onto ice, then 5 ml of concentrated hydrochloric acid are added with stirring. The mixture is extracted with 2 fractions of ethyl ether and the ethereal extracts are pooled. They are washed with 3 fractions of 30 ml of a 10% aqueous solution of sodium bicarbonate and the aqueous phase is acidified.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05028710 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-dadf82c642b3438f8c8e5e02b6292229 |
| Source note | uspto-grants-1991_07 |