Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248981Generated: October 30, 2026

Acetic Anhydride → HCID 19995349, compound

https://huagongshe.com/reaction/2248981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantPropane, 2,2',2''-[methylidynetris(oxy)]tris-HCID 78191—
ReactantDiisopropyl malonateHCID 83223—
ProductDiisopropyl malonateHCID 832237.6%
ProductHCID 19995349HCID 1999534980.2%
ProductHCID 19995351HCID 199953516.5%

Reaction Conditions

Temperature-10 °C

Reaction Steps

188 g (1 mol) of diisopropyl malonate, 571 g (3 mol) of triisopropyl orthoformate and 0.05 g of catalyst from Example 5 were initially introduced into the apparatus mentioned in Example 1 and the mixture was heated to -10° C. 102 g of acetic anhydride were then metered in over the course of 5 hours. The bottom temperature was raised to 150° C. At the same time a low-boiling fraction was removed under reflux at a boiling temperature of 60° C. After 10 hours, the formation of low-boiling component decreased. The mixture was then fractionated in vacuo, first at 15 mbar and then at 0.3 mbar. 7.6% of diisopropyl malonate, 80.2% of diisopropyl isopropoxymethylenemalonate and 6.5% of diisopropyl diisopropoxy-methylmalonate were obtained. The last-mentioned compound was converted into diisopropyl isopropoxymethylenemalonate by heating with 0.2 g of H3PO4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041619
Source datasetuspto-grants-1991_08
ORD IDord-1d3da4a9b11345e4b91dff7a76115b89
Source noteuspto-grants-1991_08