HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848688Generated: November 1, 2026
Thionyl Chloride → 2-(4-Chlorophenyl)ethyl chloride
https://huagongshe.com/reaction/1848688
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | p-Chlorophenethylic alcohol | HCID 74647 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(4-Chlorophenyl)ethyl chloride | HCID 3790359 | — |
Reaction Steps
Into a 250-mL round-bottom flask equipped with magnetic stirring, a thermocouple, a condenser, and a nitrogen bubbler vented to caustic scrubber, was charged 2-(4-chlorophenyl)ethanol (25.011 g, 160 mmol), N,N-dimethylacetamide (0.748 mL, 7.99 mmol), and toluene (73 mL). The mixture was heated to 65 to 70° C. and then thionyl chloride (12.24 mL, 168 mmol) was added over 1 h. The reaction was stirred at 60 to 68° C. for 2 h to give a dark-brown solution. This solution was cooled to 45° C., washed with water (2×27 mL) and saturated aqueous sodium bicarbonate (3×27 mL) at 40 to 45° C., and then cooled room temperature and allowed to stir overnight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08952197B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-77353034c6974a1e80f876b04a65d920 |
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| Source note | uspto-grants-2015_02 |
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