Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778392Generated: November 2, 2026

Dimethylformamide → methyl 7-tert-butylcarbonylamino-4-chloro-3-formyl-2H-chromene-8-carboxylate

https://huagongshe.com/reaction/1778392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantMethyl 7-tert-butylcarbonylamino-4-oxochroman-8-carboxylateHCID 66693192—
SolventDichloromethaneHCID 6344—
SolventTrichloroethyleneHCID 6575—
Productmethyl 7-tert-butylcarbonylamino-4-chloro-3-formyl-2H-chromene-8-carboxylateHCID 86684737—

Reaction Conditions

Temperature60 °C

Reaction Steps

A suspension of methyl 7-tert-butylcarbonylamino-4-oxochroman-8-carboxylate (Intermediate 77, 1.32 g) in trichloroethylene (25 mL) was treated with DMF (1.5 mL), followed by dropwise addition of phosphorus oxychloride (0.998 g). The resultant mixture was heated at 60° C. for 2 hours. A further amount of phosphorus oxychloride (0.200 g) was added and the mixture was heated at 60° C. for 40 minutes. After cooling, the mixture was diluted with DCM and washed with saturated aqueous sodium bicarbonate solution. The aqueous phase was extracted with DCM and the combined organic layers were washed with brine, dried (Na2SO4) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane, with a gradient of 0-25% to give methyl 7-tert-butylcarbonylamino-4-chloro-3-formyl-2H-chromene-8-carboxylate (1.175 g) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266896B2
Source datasetuspto-grants-2016_02
ORD IDord-e078fc4cc76940f58b34499b6204e383
Source noteuspto-grants-2016_02