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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485093Generated: October 31, 2026

(1-Methylcyclopropyl)methanol → HCID 118113349, compound

https://huagongshe.com/reaction/1485093

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1-Methylcyclopropyl)methanolHCID 137701—
Reactant6-Chloro-N-methoxy-N-methylnicotinamideHCID 11435597—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 118113349HCID 11811334954%

Reaction Steps

To a solution of potassium tert-butoxide (1.68 g) in tetrahydrofuran (30 mL), a solution of 1-methylcyclopropanemethanol (1.29 g) in tetrahydrofuran (5 mL) was added and the mixture was stirred at room temperature for 10 minutes. After the reaction mixture was cooled to 0° C., a solution in tetrahydrofuran (5 mL) of the compound (3.00 g) obtained in step (1) above was added and after being brought to room temperature, the reaction mixture was stirred for an hour. The reaction mixture was then concentrated under reduced pressure and the resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=95:5-50:50) to give N-methoxy-N-methyl-6-[(1-methylcyclopropyl)methoxy]pyridine-3-carboxamide as a colorless oil (2.02 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422240B2
Source datasetuspto-grants-2016_08
ORD IDord-f8eaa44371694385ae506730233af711
Source noteuspto-grants-2016_08