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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516474Generated: November 2, 2026

1,3-Dichloroacetone → tert-Butyl 4-(4-(chloromethyl)thiazol-2-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1516474

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DichloroacetoneHCID 10793—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactanttert-Butyl 4-carbamothioylpiperidine-1-carboxylateHCID 2735648—
SolventAcetoneHCID 180—
Producttert-Butyl 4-(4-(chloromethyl)thiazol-2-yl)piperidine-1-carboxylateHCID 57423790—

Reaction Steps

To a solution of 4-thiocarbamoyl-piperidine-1-carboxylic acid tert-butyl ester (4.9 g, 20 mmol) in acetone (80 mL) was added 1,3-dichloroacetone (3.3 g, 26 mmol), MgSO4 (3.6 g, 30 mmol) and MgCO3 (1.68 g, 20 mmol). The mixture was heated under reflux overnight, cooled and filtered through celite. The solvent was removed in vacuo and the residue was redissolved with EtOAc (150 mL). The resulting solution was washed successively with 5% NaHSO3, saturated NaHCO3 and brine. After drying (Na2SO4), the solvent was removed to afford the desired product. 1H NMR (CDCl3): δ 7.20 (1H, s), 4.67 (2H, s), 4.20 (2H, br), 3.16 (1H, m), 2.87 (2H, m), 2.09 (2H, m), 1.72 (2H, m), 1.47 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08227495B2
Source datasetuspto-grants-2012_07
ORD IDord-54a8e0a1426742acb32030d0142e7488
Source noteuspto-grants-2012_07