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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679874Generated: November 3, 2026

1-Penten-3-one → HCID 23458239, compound

https://huagongshe.com/reaction/1679874

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Penten-3-oneHCID 15394—
ReactantHCID 15899924HCID 15899924—
SolventChloroformHCID 6212—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 23458239HCID 2345823931.6%

Reaction Steps

The procedure of Example 2 is followed but triethylammonium pyrid-2-yldithiocarbamate (54.0 g) and pent-1-en-3-one (17.0 g) in anhydrous acetonitrile (400 cc) are used as the starting materials at a maximum temperature of 5° C. The reaction is allowed to proceed for 3 hours at between 5° and 20° C. The crude product (45.0 g) is dissolved in a mixture of chloroform (200 cc) and ethyl acetate (50 cc). The solution is chromatographed on a column of diameter 6 cm, containing silica (0.063-0.2 mm; 600 g). Elution is carried out with a mixture of chloroform (400 cc) and ethyl acetate (100 cc), this eluate being discarded, and then with a mixture of chloroform (2,800 cc) and ethyl acetate (700 cc), this eluate being collected and evaporated to dryness under reduced pressure (20 mmHg) at 45° C. The product obtained (30.0 g) is purified by recrystallisation from a mixture of acetonitrile (30 cc) and diisopropyl ether (60 cc). 3-Oxopentyl pyrid-2-yldithiocarbamate (16.0 g) (structure determined by IR spectroscopy in petroleum jelly), which melts at 80° C., is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04271156
Source datasetuspto-grants-1981_06
ORD IDord-c0755720b613405db037fe2142d4e948
Source noteuspto-grants-1981_06