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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689438Generated: October 31, 2026

Chloroacetyl chloride → tert-Butyl 4-(2-(2-chloroacetamido)ethyl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/1689438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl 4-(2-aminoethyl)-4-hydroxypiperidine-1-carboxylateHCID 45789931—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 4-(2-(2-chloroacetamido)ethyl)-4-hydroxypiperidine-1-carboxylateHCID 57989111—

Reaction Conditions

Temperature0 °C

Reaction Steps

Chloroacetyl chloride (0.483 mL) was added dropwise over 10 minutes to a vigorously stirred mixture at 0° C. of tert-butyl 4-(2-aminoethyl)-4-hydroxypiperidine-1-carboxylate (example 89, step b) (1.1 g) in ethyl acetate (25 mL) and potassium carbonate (1.77 g) dissolved in water (20 mL). The mixture was then stirred at 0° C. for 45 minutes before being extracted with ethyl acetate. The organic layer was dried over sodium sulphate, filtered and the solvent evaporated under reduced pressure. The crude product was purified by flash silica chromatography eluting with ethyl acetate. Pure fractions were evaporated to dryness to afford the subtitled compound. Yield 0.9 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148373B2
Source datasetuspto-grants-2012_04
ORD IDord-be2809e1fc6047478e5f72f7ad018828
Source noteuspto-grants-2012_04