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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379435Generated: October 30, 2026

Methanol → N-tert.-butyl-6-chloro-4-(prop-2-yl)-nicotinamide

https://huagongshe.com/reaction/379435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
ReactantN-tert-butyl-6-chloronicotinamideHCID 11816697—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
ProductN-tert.-butyl-6-chloro-4-(prop-2-yl)-nicotinamideHCID 1141414956%

Reaction Conditions

Temperature0 °C

Reaction Steps

7.0 ml (14.1 mMol) iso-Propylmagnesium chloride solution (2M in THF) were added over 5 minutes to a solution of 1.0 g (4.7 mMol) N-tert.-butyl-6-chloro-nicotinamide in 5.0 ml THF cooled to 0° C. and the reaction mixture was stirred 18 hours at room temperature. After cooling to 0° C., 1.14 ml (28.2 mMol) methanol were added over 10 minutes, followed, after 15 minutes, by 1.17 g (5.2 mMol) 2,3-dichloro-5,6-dicyano-1,4-benzoquinone. After stirring 30 minutes at room temperature, the red-brown solution was concentrated under reduced pressure to about 10 g, heated to 50° C. and 20 ml tert.-butyl-methylether were added. The resulting suspension was stirred 1 hour at 55° C., then 1 hour at room temperature and filtered. The filtrate was concentrated under reduced pressure and digested in 9 ml n-hexane/ethyl acetate 4:1 to yield 0.67 g (56%) N-tert.-butyl-6-chloro-4-(prop-2-yl)-nicotinamide as a beige powder of m.p.=130-140° C. (dec.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06297375B1
Source datasetuspto-grants-2001_10
ORD IDord-3365bc037e9f42cc9a32c83156492df0
Source noteuspto-grants-2001_10