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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975475Generated: October 31, 2026

Methane → 1-allyloxycarbonylamino-2-(N-allyloxycarbonylaminomethyl)butan-3-ol

https://huagongshe.com/reaction/1975475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantHCID 19099247HCID 19099247—
SolventMethanolHCID 887—
Product1-allyloxycarbonylamino-2-(N-allyloxycarbonylaminomethyl)butan-3-olHCID 1909930297.9%

Reaction Steps

1,2-Bis(benzyloxycarbonyl)-4-(1-hydroxyethyl)pyrazolidine (100 g) in methanol (900 ml) was treated with activated charcoal at room temperatures for 30 minutes. After removing activated charcoal platinum oxide (22 g) was added under nitrogen atmosphere. The suspension was stirred under hydrogen atmosphere for 17 hours. After the starting material and mono(benzyloxycarbonyl) compound was disappeared. The catalyst was filtered off under nitrogen atmosphere. The cake was washed with water (300 ml) and combined aqueous metanol layer was evaporated under reduced pressure. The pH of the residue and tetrahydrofuran (500 ml) was adjusted to 8.0 with 4N aqueous sodium hydroxide and allyl chloroformate was added dropwise while keeping pH at 8.0-9.0 with 4N aqueous sodium hydroxide in an ice-bath. After stirring for 1 hour at pH 8.0-8.3, the reaction mixture was extracted three times with ethyl acetate (250 ml×1 and 100 ml×2). The combined organic layer was washed with 1N hydrochloric acid, saturated sodium bicarbonate, and 10% sodium chloride, dried over magnesium sulfate and evaporated under reduced pressure. The residue was calumn chromatographed on silica gel to give 1-allyloxycarbonylamino-2-(N-allyloxycarbonylaminomethyl)butan-3-ol (72.88 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05286721
Source datasetuspto-grants-1994_02
ORD IDord-71a25af6428d47faa9b107939920b610
Source noteuspto-grants-1994_02