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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021422Generated: October 31, 2026

Potassium Carbonate → Ethyl 7-(4-(tert-butoxycarbonyl)-2-nitrophenoxy)-6,8-dichlorochroman-4-carboxylate

https://huagongshe.com/reaction/1021422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl 4-fluoro-3-nitrobenzoateHCID 58748597—
ReactantEthyl 6,8-dichloro-7-hydroxychroman-4-carboxylateHCID 67080489—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductEthyl 7-(4-(tert-butoxycarbonyl)-2-nitrophenoxy)-6,8-dichlorochroman-4-carboxylateHCID 67080485104.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of ethyl 6,8-dichloro-7-hydroxychroman-4-carboxylate (35 g, 120.22 mmol), tert-butyl 4-fluoro-3-nitrobenzoate (31.1 g, 128.93 mmol), K2CO3 (24.923 g, 180.33 mmol), and 1-methyl-2-pyrrolidinone (500 mL) was purged with Argon (bubbled through) for 15 minutes. The mixture was heated to 80° C. for 4 hours under Argon atmosphere. The mixture was cooled to ambient temperature and poured into 3 liters of water. The pH was adjusted to pH 2 by addition of concentrated HCl (4×10 ml). A solid precipitated out as HCl was added and gas evolution was observed. The crude mixture was filtered and the solid was dissolved in EtOAc (1 liter). The EtOAc solution was washed with 2N HCl solution (200 ml), water (2×200 ml), and brine (200 ml), dried over MgSO4, filtered, and concentrated to provide 64.1 g of the title compound as a dark solid (104%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716498B2
Source datasetuspto-grants-2014_05
ORD IDord-c306f1cabab144c4b3ead3ebf6ba92ea
Source noteuspto-grants-2014_05