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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579523Generated: October 30, 2026

4,4,5,5-Tetramethyl[1,3,2]dioxaborolane → 5-Ethyl-2,2-diphenyl-4-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-butyl]-oxazolidine-4-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/579523

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4,5,5-Tetramethyl[1,3,2]dioxaborolaneHCID 2734768—
Reactant4-But-3-enyl-5-ethyl-2,2-diphenyl-oxazolidine-4-carboxylic acid tert-butyl esterHCID 66833218—
CatalystChlorotris(triphenylphosphine)rhodium(I)HCID 84599—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product5-Ethyl-2,2-diphenyl-4-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-butyl]-oxazolidine-4-carboxylic acid tert-butyl esterHCID 6683321650%

Reaction Steps

A solution of 4-but-3-enyl-5-ethyl-2,2-diphenyl-oxazolidine-4-carboxylic acid tert-butyl ester (230 mg, 0.56 mmol) in dichloromethane (2 mL, 0.3 M) was added chlorotris (triphenylphosphine)rhodium(I) (60 mg, 0.065 mmol, 10 mol %) at room temperature. After stirring for 30 min, 4,4,5,5-Tetramethyl-1,3,2-dioxaborolane (200 μl, 1.3 mmol, 2 eq) was added to the reaction mixture and stirred overnight. After quenching the reaction with water (3 mL), the resulting solution was diluted with ethyl acetate and washed successively with water and saturated aqueous NaCl, dried over MgSO4, filtered and concentrated. Purification by MPLC (1-40% ethyl acetate in heptane) gave 5-Ethyl-2,2-diphenyl-4-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-butyl]-oxazolidine-4-carboxylic acid tert-butyl ester (152 mg, 0.28 mmol, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040703B2
Source datasetuspto-grants-2015_05
ORD IDord-d4949da2b35e4e6da5ec75f8c9a42fd6
Source noteuspto-grants-2015_05