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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816712Generated: November 2, 2026

Allyl chloroformate → HCID 69677633, compound

https://huagongshe.com/reaction/1816712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chloroformateHCID 18052—
Reactant4-Amino-1-butanolHCID 25868—
Reactant2,2-Dimethyl-1,3-dioxan-5-oneHCID 2733141—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 69677633HCID 69677633—

Reaction Steps

To a solution of 4-aminobutanol (630 mg), 5-oxo-2,2-dimethyl-1,3-dioxane (1.0 g) and acetic acid (1.20 ml) in MeOH (9 ml)-DMF (4 ml) was added sodium cyanoborohydride (622 mg) with stirring at ambient temperature, and the mixture was stirred at the same temperature overnight. To the reaction mixture was added dropwise a solution of allyloxycarbonyl chloride (0.97 ml) in THF (2 ml) with stirring under ice-cooling, and the mixture was stirred at the same temperature for 1 hour. To the reaction mixture were added ethyl acetate (50 ml) and n-hexane (10 ml), and the solution was washed in turn with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo. The resulting residue was chromatographed on silica gel (100 ml) eluting with a mixture of n-hexane and ethyl acetate (1:1 v/v). The fractions containing the object compound were collected and evaporated under reduced pressure to give 4-[allyloxycarbonyl-(2,2-dimethyl-1,3-dioxan-5-yl)]aminobutanol (1.04 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884868B1
Source datasetuspto-grants-2005_04
ORD IDord-fdd2292de30342538c531210dfc59259
Source noteuspto-grants-2005_04