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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497445Generated: October 30, 2026

Diethyl Ether → HCID 86680617, compound

https://huagongshe.com/reaction/1497445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantHCID 86680616HCID 86680616—
ReactantHCID 178418443HCID 178418443—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86680617HCID 8668061737%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-(4-((methoxymethoxy)methyl)phenyl)picolinaldehyde (0.36 g, 1.4 mmol) in THF (15 mL) at 0° C. was slowly added 3.0-M ethyl magnesium bromide in diethyl ether (1.4 mL, 4.2 mmol) was added. The reaction mixture was stirred at 0° C. for 3 h. After completion of the reaction by monitoring with TLC (50% EtOAc\hexane), the reaction mixture was quenched with sat'd. NH4Cl (50 mL) solution. The reaction mixture was extracted with EtOAc (3×50 mL), washed with water (2×50 mL), dried over Na2SO4 and concentrated in vacuo. The resulting residue was purified by a Biotage Isolera® One column purifier (silica gel 230-400μ) using 33% ethyl acetate in hexane and the product isolated as a yellow solid (0.15 g, 37% yield). 1H NMR (400 MHz, DMSO-d6): δ 8.76 (d, 1H), 8.04 (dd, 1H), 7.69 (d, 2H), 7.53 (d, 1H), 7.44 (d, 2H), 4.66 (s, 2H), 4.57 (s, 2H), 3.30 (s, 3H), 1.79 (m, 1H), 1.65 (m, 1H), 0.862 (t, 3H); LC-MS: m/z 288.5 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199975B2
Source datasetuspto-grants-2015_12
ORD IDord-67621a4ba3c444948bc56e2dbb77d952
Source noteuspto-grants-2015_12