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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213034Generated: October 31, 2026

Allyl bromide → HCID 69437788, compound

https://huagongshe.com/reaction/2213034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Tert-butyl 3-ethyl piperidine-1,3-dicarboxylateHCID 357727—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69437788HCID 6943778891%

Reaction Conditions

Temperature-78 °C

Reaction Steps

1-(1,1-Dimethylethyl) 3-ethyl 1,3-piperidinedicarboxylate (12.85 g, 50 mmol) in tetrahydrofuran (50 mL) was added slowly to a stirred, cooled (−78° C.) solution of potassium hexamethyldisilazide (14.96 g, 75 mmol) in tetrahydrofuran (75 mL). The mixture was stirred at −78° C. for 30 minutes, then 3-bromo-1-propene (6.49 mL, 9.07 g, 75 mmol) was added dropwise over 5 minutes. The mixture was stirred at −78° C. for 1 hour, then saturated aqueous ammonium chloride (200 mL) and water (100 mL) were added. The mixture was allowed to warm to room temperature and extracted with ethyl acetate (3×200 mL). The combined organic fractions were washed with aqueous citric acid (10%, 3×200 mL), saturated aqueous sodium hydrogen carbonate (200 mL) and brine (200 mL), dried (MgSO4) and the solvent was evaporated under reduced pressure to give to give the title compound as a pale yellow oil (13.46 g, 91%). m/z (ES+) 298 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105507B2
Source datasetuspto-grants-2006_09
ORD IDord-949caec97dda4eeaa796adebdab952c5
Source noteuspto-grants-2006_09