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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526379Generated: October 31, 2026

Diisopropylamine → HCID 71258941, compound

https://huagongshe.com/reaction/526379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactanttert-Butyl acetateHCID 10908—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-BromonicotinonitrileHCID 736793—
ReactantHCID 178418443HCID 178418443—
SolventDiethyl EtherHCID 3283—
ProductHCID 71258941HCID 7125894134.3%

Reaction Steps

Diisopropylamine (9.2 mL, 65 mmol) was added at 0° C. to a 3M solution of ethyl magnesium bromide in diethyl ether (10.9 mL, 32.7 mmol) and additional diethyl ether (20 mL). After one hour at 0° C. tert-butyl acetate (4.3 mL, 32.7 mmol) was added and stirring was continued for 30 minutes. 5-Bromopyridine-3-carbonitrile (2.0 g, 10.9 mmol) in diethyl ether (42 mL) was added at 0° C. After two hours at 0° C. saturated aqueous ammonium chloride solution was added. Phases were separated and the aqueous phase was extracted with diethyl ether. The combined extracts were washed with brine and dried over sodium sulfate. The solution was concentrated under reduced pressure and the residue was purified by chromatography on silica gel (ethyl acetate in hexane, 0 to 60%) to yield 1.12 g tert-butyl 3-amino-3-(5-bromopyridin-3-yl)prop-2-enoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09345793B2
Source datasetuspto-grants-2016_05
ORD IDord-85e5ba5a9d284d67b224e6a986e5a340
Source noteuspto-grants-2016_05