Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1590209Generated: November 3, 2026

Dimethylformamide → Diethyl 3,3-Diethoxypropane-1,1-dicarboxylate

https://huagongshe.com/reaction/1590209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDiethyl MalonateHCID 7761—
ReactantSodium hydrideHCID 24758—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
ProductDiethyl 3,3-Diethoxypropane-1,1-dicarboxylateHCID 29832879.9%

Reaction Steps

A mixture of 10.6 gms (0.25 moles) sodium hydride 57% oil dispersion and 75 mL hexane was stirred under argon for 10 minutes. The hexane solvent was replaced by 125 mL of dry dimethylformamide, and to this suspension was added dropwise 40.5 gms (0.25 moles) diethyl malonate over 30 minutes. 49 gms (0.25 moles) bromoacetaldehyde diethyl acetal was then added dropwise over 20 minutes. After the addition was complete, the reaction mixture was stirred at 86 degrees Celsius for 18 hours, then cooled to room temperature and diluted with 600 mL of an ice-water mixture. The mixture was 4×200 mL ether extracted. The ether extracts were combined, washed twice with 50 mL cold 5% HCl, twice with 50 mL 5% NaHCO3 solution, twice with saturated NaCl solution, dried over magnesium sulfate, and filtered. The ether was evaporated in vacuo to give 55.2 gms of oil. The crude oil was purified by two successive vacuum distillations to finally give 18 gms of pure product, b.p. 81-83 degrees/0.1 mmHg. Elemental analysis: calculated C 56.51, H 8.75; found C 57.11, H 9.09.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05202350
Source datasetuspto-grants-1993_04
ORD IDord-9f9eb16e9a9749b9a87a6f0c1f07bdd0
Source noteuspto-grants-1993_04