Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432034Generated: October 31, 2026

tert-Butyl bromoacetate → HCID 60684633, compound

https://huagongshe.com/reaction/1432034

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantDiisopropylethylamineHCID 81531—
ReactantPiperidin-2-ylmethanolHCID 94263—
SolventDimethylformamideHCID 6228—
ProductHCID 60684633HCID 60684633—

Reaction Conditions

Temperature50 °C

Reaction Steps

Bromo-acetic acid tert-butyl ester (0.39 g, 2 mmol) was dissolved in DMF (1 mL). A solution of piperidin-2-yl-methanol (0.25 g, 2.2 mmol) in DMF (1 mL) and diisopropylethylamine (0.38 mL, 2.2 mmol) was added. The reaction mixture was stirred at 50° C. for 16 h. The solvent was removed in vacuo. EtOAc (20 mL) and water (7 mL) was added. The two phases were separated. The aqueous phase was extracted twice with EtOAc (20 mL). The combined EtOAc phases were dried over magnesium sulfate, filtered and the filtrate was evaporated in vacuo. The product was isolated as an oil. Yield: 0.37 g, 80%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612068B2
Source datasetuspto-grants-2009_11
ORD IDord-38f18d7a1c914394ae799bd95c29cc18
Source noteuspto-grants-2009_11