HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848692Generated: October 30, 2026
Thionyl Chloride → 2-(4-Chlorophenyl)ethyl chloride
https://huagongshe.com/reaction/1848692
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | p-Chlorophenethylic alcohol | HCID 74647 | — |
| Catalyst | Dimethylacetamide | HCID 31374 | — |
| Product | 2-(4-Chlorophenyl)ethyl chloride | HCID 3790359 | 105.4% |
Reaction Steps
In a 250-mL round bottom flask equipped with overhead stirring, a thermocouple, a condenser, and a nitrogen bubbler vented to a caustic scrubber, 2-(4-chlorophenyl)ethanol (40.011 g, 255 mmol) and N,N-dimethylacetamide (1.197 mL, 12.77 mmol) were heated to 55° C. Thionyl chloride (19.58 mL, 268 mmol) was added slowly and significant off-gassing was observed. After the addition was complete the resulting dark-brown solution was stirred at between 60 and 64° C. for 1.5 hours and then allowed to cool to room temperature and stirred overnight to give the title compound as a dark-brown oil (47.060 g, including DMA and thionyl chloride).
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-83ba028f48194462ba3cce07620353d6 |
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| Source note | uspto-grants-2015_02 |
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