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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4506Generated: October 27, 2026

Neopentyl alcohol → alpha-[(2,2-Dimethylpropoxy)methyl]-1-pyrrolidineethanol

https://huagongshe.com/reaction/4506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNeopentyl alcoholHCID 6404—
ReactantEpichlorohydrinHCID 7835—
ReactantSodium HydroxideHCID 14798—
ReactantPyrrolidineHCID 31268—
Productalpha-[(2,2-Dimethylpropoxy)methyl]-1-pyrrolidineethanolHCID 1409708784.1%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a stirred mixture of 92.53 g (1.0 m) of epichlorohydrin and 88.15 g (1.0 m) of neopentyl alcohol was added 0.26 g (0.001 m) of stannic chloride. The reaction temperature rose to about 60° C. then exothermed to about 130° C. in a few seconds. The reaction mixture was stirred until the temperature receded to about 40° C. then 71.12 g (1.0 m) of pyrrolidine was added. The reaction mixture was stirred and heated to about 95° C. for 1 hr. After cooling the reaction mixture to RT, a mixture of 80 g of 50% sodium hydroxide solution and 80 g of ice was added. The reaction mixture was stirred and heated to 90° C. for 0.5 hr then cooled to RT. The reaction mixture was partitioned between 400 ml of ice water and 400 ml of ether. The organic layer was dried and concentrated in vacuo to give 181 g of oil. The oil was distilled (89°-115° C. at 0.25 mm) to give 136 g of oil that crystallized on standing, 99.1% pure by g.c.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04727072
Source datasetuspto-grants-1988_02
ORD IDord-45c157a66bd1401c8d8bebfdf83470d2
Source noteuspto-grants-1988_02