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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787914Generated: October 30, 2026

Dimethylformamide → Methyl 2-(1-tert-Butoxycarbonylpiperidin-4-yloxy)-4-(dimethylamino)benzoate

https://huagongshe.com/reaction/1787914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMorpholineHCID 8083—
ReactantCesium carbonateHCID 10796—
ReactantMethyl 2-(1-tert-Butoxycarbonylpiperidin-4-yloxy)-4-fluorobenzoateHCID 57602502—
SolventSodium chloride; waterHCID 57417360—
ProductMethyl 2-(1-tert-Butoxycarbonylpiperidin-4-yloxy)-4-(dimethylamino)benzoateHCID 5760245259%

Reaction Conditions

Temperature110 °C

Reaction Steps

The 4-dimethylamino compound was obtained in the following preparation in which the dimethylamino group was derived from in situ decomposition of the solvent DMF: A mixture of methyl 2-(1-tert-butoxycarbonylpiperidin-4-yloxy)-4-fluorobenzoate (6.45 g, 18.25 mmol), morpholine (8 g, 91.26 mmol), Cs2CO3 (11.8 g, 36.5 mmol), and DMF (10 mL) was heated 3 days at 110° C. The reaction mixture was poured into brine (100 mL) and extracted with EtOAc (3×100 mL). The combined extracts were washed with brine (3×200 mL), dried over MgSO4, and concentrated to an oil which was purified by chromatography on silica using 25% EtOAc in hexanes to give 4.1 g (59%) of product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511066B2
Source datasetuspto-grants-2009_03
ORD IDord-d3a29ac2466649be9f7409d0a2015af4
Source noteuspto-grants-2009_03