HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747272Generated: October 30, 2026
Thionyl Chloride → 5-(1-Chloroethyl)quinoline
https://huagongshe.com/reaction/747272
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-(Quinolin-5-yl)ethanol | HCID 68770902 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-(1-Chloroethyl)quinoline | HCID 59749555 | — |
Reaction Steps
The alcohol, 1-quinolin-5-yl-ethanol (5.0 g, 28.9 mmol) in chloroform was treated with a dropwise addition of thionyl chloride (5.26 mL, 72.1 mmol) at rt. After 1 h the mixture was cooled to 0° C. and carefully quenched with a sat. solution of NaHCO3 followed by 2M NaOH until the pH was >8. The aqueous layer was extracted with chloroform and the organic fractions were combined, dried over MgSO4, filtered, and freed of solvent. The residue was purified by chromatography on SiO2 eluting with 30% ethyl acetate:hexane. The product, 5-(1-chloro-ethyl)-quinoline (Intermediate E1) was obtained as a clear oil, 4.22 g (76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07396849B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-8f4aca626f2c4d9b87feb4580cca7524 |
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| Source note | uspto-grants-2008_07 |
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