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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024593Generated: October 28, 2026

1,3-Dichloro-2-propanol → 1-Dodecene

https://huagongshe.com/reaction/1024593

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dichloro-2-propanolHCID 7289—
Reactant1-DodeceneHCID 8183—
ReactantBoron trifluoride dihydrateHCID 61591—
Product1-DodeceneHCID 8183—
ProductHCID 86635908HCID 86635908—

Reaction Conditions

Temperature95 °C

Reaction Steps

To a 1000 ml round bottom flask equipped with condenser, overhead stirrer, and nitrogen inlet system is added 528 g of 1,3-dichloro-2-propanol, 6.6 g of BF3 dihydrate, and 103 g of 1-dodecene at room temperature. The mixture is heated to 95° C. for 6 hours. The reaction mixture is cooled to room temperature and is then transferred to a 1000 ml separation funnel; 200 ml of heptane is added and two phases are separated. The lower phase (containing excess dichloropropanol, ether products, unreacted and isomerized olefins, and the catalyst) is extracted with 200 ml of heptane three more times. The heptane solutions are combined and the heptane is removed on a rotary evaporator. Distillation of residual heptane under reduced pressure affords 46.3 g of dodecene isomers mixture and 94.4 g of sec-dodecyl 1,3-dichloro-2-propyl ether and isomers. The dodecene mixtures is collected at 80-105° C./0.6 mmHg, and the ether product is collected as 128-141° C./0.6 mmHg)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722944B2
Source datasetuspto-grants-2014_05
ORD IDord-e3f17a5f5b064a1ea44ce4f72ea54fd8
Source noteuspto-grants-2014_05