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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362826Generated: October 31, 2026

1,3-Dichloroacetone → HCID 86624337, compound

https://huagongshe.com/reaction/2362826

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DichloroacetoneHCID 10793—
ReactantSodium BicarbonateHCID 516892—
Reactant(4-Cyanophenyl)thioureaHCID 2757973—
ReactantHCID 178483863HCID 178483863—
SolventDimethylformamideHCID 6228—
ProductHCID 86624337HCID 86624337—

Reaction Steps

A solution of 26.6 mg (0.15 mmol) of N-(4-cyanophenyl)thiourea and 19 mg (0.15 mmol) of 1,3-dichloroacetone in 0.4 ml of DMF is stirred at +80° C. for 3 h. After cooling to RT, a solution of 50.9 mg (0.15 mmol) of the compound from Example 34A in 0.2 ml of DMF and 50 mg (0.6 mmol) of sodium bicarbonate are added. The mixture is then stirred at RT for 12 h. The reaction mixture is filtered and purified directly by preparative HPLC (column: Macherey Nagel VP50/21 Nucleosil 100-5 C18 Nautilus, 5 μm, 21 mm×50 mm; wavelength: 220 nm; flow rate: 25 ml/min; mobile phase A=water+0.1% formic acid, mobile phase B=acetonitrile; gradient: 0 min 10% B→2 min 10% B→6 min 90% B→7 min 90% B→7.1 min 10% B→8 min 10% B). The product-containing fractions are combined and concentrated using a rotary evaporator.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691850B2
Source datasetuspto-grants-2014_04
ORD IDord-11ea1f95a082427d8b7a97265932a502
Source noteuspto-grants-2014_04