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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796203Generated: November 3, 2026

Formaldehyde → HCID 22180993, compound

https://huagongshe.com/reaction/1796203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(1-t-Butoxycarbonyl-2-methylpiperidin-4-yloxy)-3-chloronitrobenzeneHCID 22181217—
SolventFormic AcidHCID 284—
ProductHCID 22180993HCID 2218099390.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a suspension of 4-(1-t-butoxycarbonyl-2-methylpiperidin-4-yloxy)-3-chloronitrobenzene (1.15 g) obtained in reference example 85 in 90% formic acid (3.10 g) was added 37% formaldehyde (2.50 g), and the resulting mixture was stirred at 100° C. for 2 hours. After cooling to room temperature, the reaction mixture was neutralized with an aqueous potassium carbonate solution and extracted with ethyl acetate. The extract was washed with a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate and evaporated in vacuo. The residue obtained was purified by chromatography on a silica gel column using a mixed solvent of dichloromethane and methanol (9:1) as the eluent to afford the title compound (0.80 g, yield: 90%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030138B2
Source datasetuspto-grants-2006_04
ORD IDord-deb1478bca3c4802b12a68bd2d9e8727
Source noteuspto-grants-2006_04