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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1974310Generated: November 2, 2026

Ammonia → 2-Pyridinemethanol, 3,4-dimethyl-alpha-(3,4,5-trimethoxyphenyl)-

https://huagongshe.com/reaction/1974310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
Reactant3,4,5-TrimethoxybenzaldehydeHCID 6858—
Reactant2-Bromo-3,4-dimethylpyridineHCID 21822291—
ReactantButyllithiumHCID 178418339—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
Product2-Pyridinemethanol, 3,4-dimethyl-alpha-(3,4,5-trimethoxyphenyl)-HCID 304448196%

Reaction Conditions

Temperature-40 °C

Reaction Steps

40 g of 2-bromo-3,4-dimethylpyridine dissolved in 50 ml of anhydrous ether are slowly added, with agitation and under a nitrogen atmosphere, to 300 ml of a 0.9 M solution of butyl-lithium in ether cooled to -40° C. The resulting mixture is agitated for 2 hours at this temperature, and 50 g of 3,4,5-trimethoxybenzaldehyde dissolved in 200 ml of anhydrous benzene are added, and the mixture kept at a temperature below -25° C. Agitation is performed for 1 hour at -15° C, and the reaction is continued until ambient temperature is reached. The mixture is poured on to ice and dilute hydrochloric acid, the acid layer is made alkaline with a current of ammonia, while cooling externally with ice. The precipitate is collected by filtration, supplying 62.6 g of (II). Yield 96%. An analysis sample is crystallized from alcohol (m.p. = 104-6° C). Analysis: C17H21NO4. Calculated: C = 67.31, H = 6.98, N = 4.62. Found: C = 67.23, H = 7.33, N = 4.57.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04000283
Source datasetuspto-grants-1976_12
ORD IDord-1ba60369a52240a9a98f672284bfb9b7
Source noteuspto-grants-1976_12