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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467148Generated: October 29, 2026

HCID 14299925, compound → HCID 11658392, compound

https://huagongshe.com/reaction/467148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 14299925HCID 14299925—
ReactantHydrochloride methanolHCID 21893726—
ProductHCID 11658392HCID 11658392—

Reaction Steps

tert-Butoxycarbonyl-L-prolinal dimethyl acetal (1.0 g, 4.08 mmol) is stirred for one hour at room temperature in 10% HCl-methanol (8.2 ml) and the mixture is evaporated to dryness under reduced pressure to give quantitatively L-prolinal dimethylacetal hydrochloride as a solid. The product is dissolved in dimethylformamide (5 ml) containing p-anisic acid (938 mg, 6.16 mmol) and diethyl-phosphoryl cyanide (0.65 ml, 8.25 mmol). To the solution is added dropwise triethylamine (1.15 ml, 8.25 mmol) under cooling and agitation in an ice-methanol bath. After the dropwise addition the mixture is stirred for one hour under cooling and then for one hour at room temperature. Benzene-ethyl acetate (2:1, 150 ml) is added to the reaction mixture and the organic layer was separated, washed successively with a saturated aqueous solution of sodium hydrogen carbonate (15 ml), water (15 ml) and a saturated aqueous solution of edible salt (15 ml), dried over sodium sulfate and filtered. The filtrate is concentrated to dryness under reduced pressure. The residue is purified by column chromatography on silica gel (n-hexane-dichloromethanemethanol, 6:4:1) to give 747 mg (65%) of the title compound as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05158970
Source datasetuspto-grants-1992_10
ORD IDord-18d09b3d7ba74b7881f1434751a86429
Source noteuspto-grants-1992_10