Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493559Generated: October 30, 2026

Boron trifluoride etherate → Bicyclo[3.3.1]nonane, 2-ethoxy-2,6,6-trimethyl-9-methylene-

https://huagongshe.com/reaction/1493559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl orthoformateHCID 31214—
ReactantDihydro-alpha-iononeHCID 35821—
SolventEthanolHCID 702—
ProductBicyclo[3.3.1]nonane, 2-ethoxy-2,6,6-trimethyl-9-methylene-HCID 11137697.8%

Reaction Steps

480 g (2.21 mol) of dihydro-α-ionone, 368 g (2.48 mol) of triethyl orthoformate and 480 ml of abs. ethanol are treated dropwise while stirring during 15 minutes with a solution of 34.5 g (0.31 mol) of boron trifluoride etherate in 500 ml of ethanol and the mixture is subsequently heated to an internal temperature of 46°-48° for 60 minutes. After cooling the reaction mixture to room temperature it is stirred with 600 ml of a 10% aqueous sodium hydroxide solution. After extraction with ether and evaporation of the organic phase there are obtained 668.7 g of a slightly yellow liquid which, after flash distillation in a vacuum, gives 480.5 g of crude product (b.p. 45°-73°, 0.07 mbar). After fractionation in a vacuum over a 20 cm Widmer column there are obtained 406.2 g (82.7% of theory) of a slightly yellowish colored liquid (b.p. 48°-67°, 0.06 mbar) which contains the desired bicyclo-nonane in an isomer ratio of exo:endo=2:1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05023232
Source datasetuspto-grants-1991_06
ORD IDord-9b8b3c76b67a4e78a9cef974334e19ba
Source noteuspto-grants-1991_06