Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1105739Generated: October 29, 2026

Propargyl bromide → Heptopargil

https://huagongshe.com/reaction/1105739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantCamphor oximeHCID 26110—
ReactantSodiumHCID 5360545—
SolventMethanolHCID 887—
ProductHeptopargilHCID 5269281%

Reaction Steps

4.6 g (0.2 mole) of metallic sodium are dissolved in 200 ml of methanol, and 33.4 g (0.2 mole) of (±)-1,7,7-trimethyl-bicyclo[2,2,1]heptane-2-one-oxime are added to the solution. After one hour of boiling 23.8 g (0.2 mole) of propargyl bromide are introduced, and the reaction is continued for a further hour. The mixture is cooled, the separated sodium bromide is filtered off, the filtrate is concentrated, and the concentrate is subjected to fractional distillation in vacuo. 33.2 g (81%) of (±)-2-(propargyloxyimino)-1,7,7-trimethyl-bicyclo[2,2,1]heptane are obtained as a light yellow oil; b.p.: 94° C./1.5 mm Hg, nD20 =1.4955.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04310348
Source datasetuspto-grants-1982_01
ORD IDord-31ba1d9b56c24c278401acfbe1f230e5
Source noteuspto-grants-1982_01