HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl diazoacetate → (1S,1aS,6bR)-Ethyl-5-((tert-butyldimethylsilyl)oxy)-1a,6b-dihydro-1H-cyclopropa[b]benzofuran-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl diazoacetate | HCID 12192 | — |
| Reactant | (Benzofuran-5-yloxy)(tert-butyl)dimethylsilane | HCID 68968953 | — |
| Catalyst | Copper(I) trifluoromethanesulfonate | HCID 9813164 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (1S,1aS,6bR)-Ethyl-5-((tert-butyldimethylsilyl)oxy)-1a,6b-dihydro-1H-cyclopropa[b]benzofuran-1-carboxylate | HCID 131734886 | 108% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09273046B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-94fef5bf7c0a448d9ce3925a8c7333c5 |
| Source note | uspto-grants-2016_03 |