HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602221Generated: October 29, 2026
Acetic Acid → 1-Hexanol, 6-chloro-, 1-acetate
https://huagongshe.com/reaction/602221
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 6-Chloro-1-hexanol | HCID 74828 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-Hexanol, 6-chloro-, 1-acetate | HCID 170285 | — |
Reaction Steps
6-chlorohexanol (800 g) was added to anhydrous acetic acid (1,200 mL) cooled to 10° C. in an ice bath, and then pyridine (934 g) was dropped for 10 minutes. After the completion of dropping, they were refluxed for 2 hours. The reaction mixture was poured into water and toluene was further added and stirred. After neutralization the toluene layer with an aqueous saturated solution of sodium carbonate, it was washed with a small amount of water and further dried over anhydrous magnesium sulfate. Toluene and unreacted ingredients were distilled off from the toluene layer to obtain concentrates. The concentrates were purified by distillation under a reduced pressure to obtain 6-acetoxy chlorohexane (983 g). The boiling point was 82° C./5.3 hPa.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE042221E1 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-b8374db747bd4a80b17fb2f2af04a106 |
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| Source note | uspto-grants-2011_03 |
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