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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478152Generated: October 31, 2026

Dichloromethane → Ethyl 4-methyl-5-(spiro[4.5]dec-7-en-8-yl)isoxazole-3-carboxylate

https://huagongshe.com/reaction/1478152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
Reactant4,4,5,5-Tetramethyl-2-(spiro[4.5]dec-7-EN-8-YL)-1,3,2-dioxaborolaneHCID 23141576—
ReactantEthyl 5-bromo-4-methyl-1,2-oxazole-3-carboxylateHCID 58828802—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductEthyl 4-methyl-5-(spiro[4.5]dec-7-en-8-yl)isoxazole-3-carboxylateHCID 118511037—

Reaction Steps

To a 2-5 mL microwave vial containing a solution of 4,4,5,5-tetramethyl-2-(spiro[4.5]dec-7-en-8-yl)-1,3,2-dioxaborolane (168 mg, 0.641 mmol) in MeCN (2 mL), ethyl 5-bromo-4-methylisoxazole-3-carboxylate (Intermediate A) (150 mg, 0.641 mmol) was added followed by K2CO3 (266 mg, 1.923 mmol), PdCl2(dppf).CH2Cl2 adduct (Alfa Aesar) (52.3 mg, 0.064 mmol) and water (1 mL). The vial was flushed with nitrogen, sealed and treated in the microwave (Biotage Smith Initiator) at 90° C. for 1 hour. The reaction mixture was partitioned between water (20 mL) and EtOAc (20 mL) and the organic phase was washed with brine (20 mL), dried over MgSO4, filtered and concentrated under reduced pressure to give an orange oil. The crude material was adsorbed onto silica and purification by chromatography eluting with 0-30% EtOAc in iso-hexane afforded the title compound;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403810B2
Source datasetuspto-grants-2016_08
ORD IDord-46be4304ecb1432689237f5edfee5083
Source noteuspto-grants-2016_08