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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380118Generated: October 30, 2026

Ethyl Acetate → 2-[2-(4,5-Diphenyloxazol-2-yl)pyrrolidin-1-yl]-5-tert-butyldiphenylsilyloxy-1,2,3,4-tetrahydronaphthalen

https://huagongshe.com/reaction/380118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-(4,5-Diphenyloxazol-2-yl)pyrrolidineHCID 18367276—
Reactant5-Tert-butyldiphenylsilyloxy-2-oxo-1,2,3,4-tetrahydronaphthaleneHCID 18367369—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-[2-(4,5-Diphenyloxazol-2-yl)pyrrolidin-1-yl]-5-tert-butyldiphenylsilyloxy-1,2,3,4-tetrahydronaphthalenHCID 1836724099.7%

Reaction Steps

To a solution of 2-(4,5-diphenyloxazol-2-yl)pyrrolidine (0.6 g) and 5-tert-butyldiphenylsilyloxy-2-oxo-1,2,3,4-tetrahydronaphthalene (0.5 g) in a mixture of methanol (10 ml) and acetic acid (2 ml) was added NaBH3CN (250 mg) at room temperature. After being stirred for 2 hours at the same temperature, the mixture was poured into the mixture of ethyl acetate and water. The organic layer was washed with water and brine, dried over MgSO4, and evaporated in vacuo. The residue was purified by chromatography on silica gel to afford 2-[2-(4,5-diphenyloxazol-2-yl)pyrrolidin-1-yl]-5-tert-butyldiphenylsilyloxy-1,2,3,4-tetrahydronaphthalen (0.84 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300344B1
Source datasetuspto-grants-2001_10
ORD IDord-e9252b978caf410e81ba4542f135cc4c
Source noteuspto-grants-2001_10