Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908805Generated: October 28, 2026

Ethyl 6-chloro-4-methylpyridine-2-carboxylate → HCID 66933544, compound

https://huagongshe.com/reaction/1908805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 6-chloro-4-methylpyridine-2-carboxylateHCID 46835592—
CatalystHCID 178418397HCID 178418397—
SolventDiethyl EtherHCID 3283—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventPotassium CarbonateHCID 11430—
ProductHCID 66933544HCID 6693354464%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of ethyl 6-chloro-4-methyl-pyridine-2-carboxylate (500 mg, 2.51 mmol) and 2,4,6-tris-(2-methyl-propenyl)-cyclotriboroxane pyridine complex (814 mg, 2.51 mmol) in DME (32 mL), 2 M aq. K2CO3 (12 mL) solution is added. The mixture is degassed and put under argon before Pd(PPh3)4 (52 mg, 0.045 mmol) is added. The mixture is stirred at 80° C. for 6 h before it is cooled to rt, diluted with diethyl ether (50 mL) and washed with sat. aq. NaHCO3 (2×30 mL) solution. The org. extract is dried over MgSO4, filtered and concentrated. The crude product is purified by CC on silica gel eluting with heptane:EA 9:1 to give 4-methyl-6-(2-methyl-propenyl)-pyridine-2-carboxylic acid ethyl ester (176 mg) as a yellow oil; 1H NMR (CDCl3): δ 1.45 (t, J=7.0 Hz, 3H), 1.97 (s, 3H), 2.12 (s, 3H), 2.42 (s, 3H), 4.46 (q, J=7.0 Hz, 2H), 6.41 (s, 1H), 7.17 (s, 1H), 7.75 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598208B2
Source datasetuspto-grants-2013_12
ORD IDord-c626c09eba8546dfb8bcdf4f61e1a96b
Source noteuspto-grants-2013_12