HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477332Generated: October 26, 2026
Ethanol → Ethyl (4-methylbenzylthio)acetate
https://huagongshe.com/reaction/477332
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | p-Xylyl bromide | HCID 7721 | — |
| Reactant | Ethyl Thioglycolate | HCID 12185 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl (4-methylbenzylthio)acetate | HCID 4107274 | — |
Reaction Steps
Ethyl 2-mercaptoacetate (8.5 cc) is added in the course of 15 minutes at a temperature in the region of 20° C. to a stirred solution, through which a stream of nitrogen is passed, of a 2M ethanolic solution of sodium ethylate (37.5 cc) and ethanol (50 cc). The mixture is left with stirring for 15 minutes at the same temperature, and α-bromo-p-xylene (13.9 g) is then added in the course of 20 minutes at a temperature in the region of 20° C. Stirring is maintained for 60 minutes at this temperature, and the reaction mixture is then evaporated to dryness at 50° C. under reduced pressure (20 mm Hg; 2.7 kPa). The residue obtained is dissolved in dichloromethane (100 cc), and the organic phase is dried over anhydrous magnesium sulphate, filtered and concentrated to dryness at 40° C. under reduced pressure (20 mm Hg; 2.7 kPa). Ethyl (4-methylbenzylthio)acetate (15.6 g) is thereby obtained, and is used in the crude state in the subsequent syntheses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04886835 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-5f945fb988944ca2b579be667497689b |
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| Source note | uspto-grants-1989_12 |
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