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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185567Generated: October 31, 2026

1,2-Dimethoxyethane → HCID 22458227, compound

https://huagongshe.com/reaction/2185567

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 22458230HCID 22458230—
ReactantHCID 178418676HCID 178418676—
SolventDiethyl EtherHCID 3283—
ProductHCID 22458227HCID 2245822769%

Reaction Conditions

Temperature0 °C

Reaction Steps

N-Methyl-N-methoxy-3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propionamide (550 mg, 1.83 mmol, from Step B) was dissolved in 10 mL dry ether and the solution was cooled to 0° C. A solution of 4-fluorophenyl magnesium bromide (2 mL, 1.0 M in THF, 2.01 mmol) was added dropwise. A solid mass formed upon addition and 1 mL 1,2-dimethoxyethane was added. The mixture was warmed to room temperature and stirred for 45 min then poured into 100 mL EtOAc/10 mL 1 M aqueous HCl. The layers were separated and the organic phase was washed with water, then sat'd NaCl, then dried over Na2SO4 and concentrated. Flash chromatography (25 grams silica, 5/1 hexane/EtOAc eluant) afforded 423 mg (69%) of the title compound. 1H NMR (300 MHz, CDCl3) δ1.0-1.20 (m, 2H), 1.45 (s, 9H), 1.65-1.75 (m 4H), 2.6-2.75 (m 2H), 2.9-3.0 (t, 2H), 4.03-4.08 (m, 2H), 7.1-7.19 (m, 2H), 7.95-8.04 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399619B1
Source datasetuspto-grants-2002_06
ORD IDord-520bc885782c4463832b054746f8d8c1
Source noteuspto-grants-2002_06