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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74324Generated: November 4, 2026

Pyridine → HCID 86762710, compound

https://huagongshe.com/reaction/74324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDimethylformamideHCID 6228—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 86762709HCID 86762709—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
ProductHCID 86762710HCID 8676271089.4%

Reaction Conditions

Temperature7.5 °C

Reaction Steps

(Z,Z,E)-3,7,9-Dodecatrien-1-ol (169.47 g, 0.94 mol), pyridine (134.2 g, 1.70 mol) and N,N-dimethylformamide (284 g) were placed in a reaction vessel, and stirred at 5 to 10° C. for 30 minutes. After stirring, methanesulfonyl chloride (151.2 g, 1.32 mol) was added dropwise thereto at 5 to 15° C. After completion of the dropwise addition, the reaction mixture was stirred at 60 to 65° C. for 2 hours. Then, water (471 g) was added to the reaction mixture to terminate the reaction. Hexane (471 g) was added thereto to separate the reaction mixture into phases. The organic phase was washed with hydrochloric acid and then with an aqueous sodium bicarbonate solution, and then concentrated by removal of the solvent under reduced pressure. The residue was distilled under reduced pressure to obtain (Z,Z,E)-1-chloro-3,7,9-dodecatriene (bp: 114 to 120° C./5 mmHg, 166.93 g, 0.84 mol) with a yield of 89.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829255B1
Source datasetuspto-grants-2014_09
ORD IDord-35ca9c29b0764a1cadceb029af52b8c9
Source noteuspto-grants-2014_09