HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-(1H-Inden-3-yl)ethyl 4-methylbenzenesulphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 1H-Indene-3-ethanol | HCID 11355648 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-(1H-Inden-3-yl)ethyl 4-methylbenzenesulphonate | HCID 12178095 | 71.8% |
Reaction Steps
5 g (0.031 mol) of 1H-indene-3-ethanol are dissolved in 50 ml of dry pyridine. The mixture is stirred and cooled using an ice bath, 5.9 g (0.031 mol) of 4-methylbenzenesulphonyl chloride are added in portions, and stirring is continued under cold conditions for 1 h and then at room temperature for 4 h. The solution obtained is poured into a mixture of 100 ml of 10N hydrochloric acid and 200 g of ice. The mixture is extracted twice with diethyl ether, and the organic phase is separated, washed with water, dried over magnesium sulphate and filtered. The filtrate is evaporated under reduced pressure. 7 g of an oily product are obtained which is used as it is in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05530002 |
| Source dataset | uspto-grants-1996_06 |
| ORD ID | ord-88934561421c4dcca73a81f1e7b58d0e |
| Source note | uspto-grants-1996_06 |