Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358902Generated: October 25, 2026

Water → tert-Butyl 3-methylidenepyrrolidine-1-carboxylate

https://huagongshe.com/reaction/358902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanttert-Butyl 3-((tosyloxy)methyl)pyrrolidine-1-carboxylateHCID 20067158—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 3-methylidenepyrrolidine-1-carboxylateHCID 1529796743.1%

Reaction Steps

2.24 g (0.02 mole) of potassium t-butoxide were added to a solution of 3.55 g (0.01 mole) of 1-t-butoxycarbonyl-3-(p-toluenesulfonyloxymethyl)pyrrolidine [prepared as described in Step (3) above] dissolved in 50 ml of tetrahydrofuran. The mixture was then stirred at room temperature for 3 hours, after which it was poured into water and then extracted with ethyl acetate. The ethyl acetate extract was washed with water, dried and concentrated by evaporation under reduced pressure. The residue was subjected to column chromatography through silica gel eluted with a 5:95 by volume mixture of ethyl acetate and toluene, to give 0.79 g of 1-t-butoxycarbonyl-3-methylenepyrrolidine as a pale yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04997943
Source datasetuspto-grants-1991_03
ORD IDord-12d7f5139a684275b89d8c6b165a3f2b
Source noteuspto-grants-1991_03