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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766893Generated: October 26, 2026

Dimethylformamide → Allyl 4-[(4-methoxybenzyl)oxy]-4-oxobutyl succinate

https://huagongshe.com/reaction/1766893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant4-Methyloxybenzyl chlorideHCID 69993—
ReactantAllyl 4-chloro-4-oxobutyrateHCID 17862495—
ReactantSodium OxybateHCID 23663870—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductAllyl 4-[(4-methoxybenzyl)oxy]-4-oxobutyl succinateHCID 5888531870%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a suspension of commercially available sodium 4-hydroxybutyrate (756 mg, 6.00 mmol) in N,N-dimethylformamide (10 ml) was added 4-methoxybenzyl chloride (987 mg, 6.30 mmol), and the mixture was heated at 100° C. for 3 hours. The reaction mixture was cooled, and allyl 4-chloro-4-oxobutyrate (1.06 g, 6.02 mmol) obtained from Example 14-(1), triethylamine (920 μl, 6.60 mmol), and 4-(N,N-dimethylamino)pyridine (10 mg) were added thereto at 0° C. The mixture was stirred at room temperature for 18 hours, and the obtained mixture was diluted with ethyl acetate, then the resulting solution was washed successively with water, a saturated aqueous solution of sodium hydrogen carbonate, a saturated aqueous solution of ammonium chloride, and an aqueous solution of sodium chloride. The solution was dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure to give an oily residue. The residue was subjected to chromatography on a silica gel (50 g) column (eluent; hexane:ethyl acetate=3:1˜2:1) to afford the title compound (1.52 g, 70% yield) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230023B2
Source datasetuspto-grants-2007_06
ORD IDord-6a6751f01a83454a82f29511a6fe7c60
Source noteuspto-grants-2007_06