HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257549Generated: October 30, 2026
Hydrochloric Acid → 1-(4-Benzylthiophenyl)-2-(2-chloroethoxy)ethanol
https://huagongshe.com/reaction/2257549
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Benzylthiobenzaldehyde | HCID 53758908 | — |
| Reactant | HCID 178478511 | HCID 178478511 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-Benzylthiophenyl)-2-(2-chloroethoxy)ethanol | HCID 53756214 | — |
Reaction Steps
1.19 g of 4-benzylthiobenzaldehyde was dissolved in 20 ml of tetrahydrofuran. The solution was cooled to -10° C. Thereto was dropwise added 10 ml of a tetrahydrofuran solution containing 2M of 2-chloroethoxymethylmagnesium chloride in 10 minutes. The resulting mixture was stirred for 1 hour with ice cooling. The reaction mixture was added to a mixture of 50 ml of ice water, 50 ml of ethyl acetate and 1 g of ammonium chloride. The resulting mixture was adjusted to pH 2 with 6N hydrochloric acid. The organic layer was separated, washed with water and a saturated aqueous sodium chloride solution in this order, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue thus obtained was purified by column chromatography [eluant:toluene/ethyl acetate=20/1] to obtain 1.34 g of 1-(4-benzylthiophenyl)-2-(2-chloroethoxy)ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05658904 |
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| Source dataset | uspto-grants-1997_08 |
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| ORD ID | ord-d2341676d015406cbe04fe3c612f1add |
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| Source note | uspto-grants-1997_08 |
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