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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493296Generated: October 31, 2026

Diethyl Malonate → HCID 70448088, compound

https://huagongshe.com/reaction/1493296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantSodium hydrideHCID 24758—
ReactantHCID 70447080HCID 70447080—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 70448088HCID 70448088—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of diethyl malonate (0.64 g.) in dimethylformamide (10 ml.) was added to a stirred suspension of sodium hydride (0.14 g. of a 50% suspension in mineral oil) in dimethylformamide (10 ml.) which was maintained under an atmosphere of argon, and the mixture was stirred and heated to 50° C. for 5 minutes and then cooled to laboratory temperature. 10-[(1RS, 2RS)-5-Methoxy-2-p-methoxyphenylindan-1-yl]decyl bromide (1.2 g.) was added and the mixture was stirred at laboratory temperature for 16 hours and then diluted with water and extracted with diethyl ether. The extract was dried and evaporated to dryness and a solution of the residue (1.47 g.) in ethanol (10 ml.) was added dropwise to a stirred solution of potassium hydroxide (1.4 g.) in water (10 ml.) which was heated under reflux. The mixture was stirred and heated under reflux for 10 minutes, diluted with water and extracted with diethyl ether. The aqueous solution was acidified with concentrated aqueous hydrochloric acid and extracted with diethyl ether, and the extract was dried and evaporated to dryness. There was thus obtained as residue 12-[(1RS, 2RS)-5-methoxy-2-p-hydroxyphenylindan-1-yl]dodecanoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05021414
Source datasetuspto-grants-1991_06
ORD IDord-8b0d2f2f5d5a4b8ab2aed8e6636044d2
Source noteuspto-grants-1991_06