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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921672Generated: October 30, 2026

Dimethylformamide → Allyl (1-{4-[dihydroxy-(2-oxobenzofuran-3-ylidene)methyl]phenyl}cyclopropyl)-carbamate

https://huagongshe.com/reaction/1921672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant2(3H)-BenzofuranoneHCID 68382—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant4-(1-{[(Prop-2-en-1-yloxy)carbonyl]amino}cyclopropyl)benzoic acidHCID 59305810—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
ProductAllyl (1-{4-[dihydroxy-(2-oxobenzofuran-3-ylidene)methyl]phenyl}cyclopropyl)-carbamateHCID 131729705—

Reaction Steps

0.8 g of 4-(1-allyloxycarbonylaminocyclopropyl)benzoic acid and 0.585 mL of triethylamine were dissolved in 10 mL of anhydrous DMF and combined with 1.16 g of TBTU, stirred for 15 minutes at RT, then combined with 0.4 g of coumaranone and stirred for a further 10 minutes. While cooling with the ice bath, 0.42 g of NaH was added batchwise as a 60% suspension in white oil, the mixture was stirred for 2 hours at RT and, once the reaction had ended, the mixture was diluted with water to a total volume of approximately 150 mL. The mixture was acidified with 2N acetic acid. The crystals were suction filtered and washed with water. Yield: 1.1 g of solid with a melting point of 125° C.-126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173699B2
Source datasetuspto-grants-2012_05
ORD IDord-e23e4cda0c624d55ba0ad7ce5b26d6f4
Source noteuspto-grants-2012_05