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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967998Generated: November 2, 2026

Acetone → HCID 22291309, compound

https://huagongshe.com/reaction/967998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantHCID 21912379HCID 21912379—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22291309HCID 22291309—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of [2-(4-bromo-2,6-dimethyl-phenoxy)-3,6-dimethyl-pyridin-4-yl]-(1-ethyl-propyl)-amine in dry THF was added n-butylithium at −78° C. After stirring at −78° C. for 10 min, acetone was added and the resulting mixture was stirred at −78° C. for 30 min, the dry-ice bath was removed. After stirring for 5 min, the mixture was quenched with brine and extracted with ethyl acetate. The organic layer was separated, dried, and concentrated to dryness. The residue was purified through silica gel chromatography to give the title compound. 1H NMR(CDCl3) d 7.17(s, 2H), 6.08(s, 1H), 3.73(d, 1H), 3.33(m, 1H), 2.19(s, 3H), 2.15(s, 3H), 2.12(s, 6H), 1.4-1.7(m, 4H), 1.26(s, 6H), 0.96(t, 6H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06956047B1
Source datasetuspto-grants-2005_10
ORD IDord-5e7109dc1846427eb1e23076f2034d09
Source noteuspto-grants-2005_10