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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418975Generated: November 1, 2026

Boron trifluoride etherate → 1,1,3,3-Tetraethoxy-2-methylpropane

https://huagongshe.com/reaction/2418975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantEthyl orthoformateHCID 31214—
ReactantMethanol, 1,1-diethoxy-, 1-acetateHCID 84166—
ReactantEthyl propenyl ether ethanolHCID 86734813—
SolventDiethyl EtherHCID 3283—
Product1,1,3,3-Tetraethoxy-2-methylpropaneHCID 8276192%

Reaction Conditions

Temperature5 °C

Reaction Steps

A solution of one equivalent of diethoxymethyl acetate and one equivalent of a ethyl propenyl ether/ethanol mixture is stirred at ambient temperature for 30 min. followed by the addition of 1.3 equivalents of triethyl orthoformate. After cooling to 5° C. 1.5 ml. of boron trifluoride etherate is added and the resulting exotherm (5° to 37° C.) is controlled with an ice bath. After stirring at ambient temperature overnight the yellow reaction solution is diluted with ether and washed with water, saturated aqueous sodium bicarbonate and again with water. Drying (MgSO4) followed by solvent removal afforded a 92% yield of oil which is shown by glc to be ~80% pure product, δ(TMS, CDCl3) 4.44 (d, 2H, CH--O); 3.3-4.0 (complex, 8H, ethyl methylene, ~2.1 (m, 1H, CH3--CH), 1.1 (t, 12H, ethyl methyls), and 1.0 (d, 3H, CH3 --CH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04104273
Source datasetuspto-grants-1978_08
ORD IDord-9e90f11d46334ee1bd4f6018e5eb5fb3
Source noteuspto-grants-1978_08