HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2985Generated: October 28, 2026
Pyridine → 6,8-dichlorooctanoic Acid
https://huagongshe.com/reaction/2985
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 8-Chloro-6-hydroxyoctanoic acid | HCID 10954458 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6,8-dichlorooctanoic Acid | HCID 9964447 | — |
Reaction Steps
To a solution of 2.4 g (12.3 mmoles) of (+)-8-chloro-6-hydroxy-octanoic acid (+)-(VI) and 0.05 g (0.6 mmoles) of pyridine in 30 ml toluene, 3.3 g (27.7 mmoles) of thionyl chloride were added slowly. The mixture was then refluxed for 1 hour. The reaction mixture was cooled to room temperature and added to 50 ml ice water. The organic phase was then removed, washed with 20 ml water and stirred for 4 hours with 30 ml of 2N NaOH. The aqueous phase was then removed, adjusted to a pH of 1 with 3N HCl and extracted twice with 20 ml diethylether. The combined ether extracts were dried over magnesium sulfate. After that, the solvent was evaporated under vacuum. (-)-6,8-dichloro-octanoic acid (-)-(VII) was obtained in a yield of 2.1 g (80% of the theoretical yield). [α]D20 =-30.6° (c=1; benzene).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05731448 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-bc41cd91f23e45a6ab06f2b380bb0c6e |
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| Source note | uspto-grants-1998_03 |
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