Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987119Generated: October 27, 2026

1,1,3,3-Tetramethylguanidine → 3-(3-Benzyloxyphenyl)-2-ethoxyacrylic acid ethyl ester

https://huagongshe.com/reaction/987119

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,3,3-TetramethylguanidineHCID 66460—
Reactant3-BenzyloxybenzaldehydeHCID 74342—
ReactantPhosphonium, (1,2-diethoxy-2-oxoethyl)triphenyl-, chloride (1:1)HCID 11327835—
SolventDichloromethaneHCID 6344—
Product3-(3-Benzyloxyphenyl)-2-ethoxyacrylic acid ethyl esterHCID 5403138169%

Reaction Steps

Tetramethylguanidine (6.5 g; 56.6 mmole) was slowly added to a solution of 3-benzyloxybenzaldehyde (11.7 g; 55 mmole) and (1,2-diethoxy-2-oxoethyl)(triphenyl) phosphonium chloride (20.1 g; 46.8 mmole) in dichloromethane (200 ml) at 0° C. After stirring at room temperature overnight the solvent was evaporated in vacuo. Diethyl ether was added and insoluble material was filtered off. The filtrate was washed with sodium bicarbonate solution, dried (magnesium sulfate), filtered and the solvent was evaporated in vacuo. The residue was purified by chromatography on silica gel using THY (0.5%) in dichloromethane as eluant. The remaining aldehyde was removed by stirring with sodium bisulfite in water and diethyl ether for 2 days. The phases were separated and the organic phase was evaporated in vacuo to give 10.5 g (yield 69%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06630509B2
Source datasetuspto-grants-2003_10
ORD IDord-dd8559a077174b7d8b287ad94b0bc7c5
Source noteuspto-grants-2003_10