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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920112Generated: November 2, 2026

Ethyl diazoacetate → (1S,1aS,6bR)-Ethyl-5-((tert-butyldimethylsilyl)oxy)-1a,6b-dihydro-1H-cyclopropa[b]benzofuran-1-carboxylate

https://huagongshe.com/reaction/920112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl diazoacetateHCID 12192—
Reactant(Benzofuran-5-yloxy)(tert-butyl)dimethylsilaneHCID 68968953—
CatalystCopper(I) trifluoromethanesulfonateHCID 9813164—
SolventDichloromethaneHCID 6344—
Product(1S,1aS,6bR)-Ethyl-5-((tert-butyldimethylsilyl)oxy)-1a,6b-dihydro-1H-cyclopropa[b]benzofuran-1-carboxylateHCID 131734886108%

Reaction Steps

Copper (I) triflate (2:1 complex with toluene, 250 mg, 2.4%) and (S,S)-(±)-2,2-isopropylidenebis(4-tert-butyl)-2-oxazoline (205 mg, 3.4%) were stirred in dichloromethane (15 mL) at ambient temperature under N2 atmosphere for 1 hour. A solution of (benzofuran-5-yloxy)(tert-butyl)dimethylsilane (5.0 g, 20.2 mmol) in dichloromethane (85 mL) was added, followed by a slow addition of ethyl diazoethanoate (40 mL, 380 mmol) during a period of 10 hours using a syringe pump. The mixture was concentrated and purified by column chromatography to afford crude compound (7.3 g) which was used for the next step without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273046B2
Source datasetuspto-grants-2016_03
ORD IDord-94fef5bf7c0a448d9ce3925a8c7333c5
Source noteuspto-grants-2016_03