Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898580Generated: November 2, 2026

2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → HCID 58438635, compound

https://huagongshe.com/reaction/1898580

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5017741—
ReactantHCID 57516630HCID 57516630—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58438635HCID 5843863581%

Reaction Conditions

Temperature-78 °C

Reaction Steps

3-(3-Bromo-phenyl)-3-aza-bicyclo[3.1.0]hexane (2.0 g, 8.4 mmol) was dissolved in 40 mL of THF and cooled to −78° C. in a dry ice acetone bath. tert-Butyl lithium (1.7 M solution in pentane, 14.8 mL, 25.2 mmol) was added dropwise and the reaction was stirred at −78° C. for 15 min. 2-Isopropoxy-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (3.4 mL, 16.8 mmol) was added and the reaction was stirred at −78° C. for 2 h. The reaction was quenched with saturated aqueous ammonium chloride and warmed to room temperature. Water was added and the layers were separated. The aqueous layer was extracted twice with ethyl acetate. The combined organic layers were dried, filtered and concentrated. The crude residue was chromatographed using a gradient of 0% to 10% ethyl acetate/heptane to give 1.93 g (81%) of 3-[3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-3-aza-bicyclo[3.1.0]hexane as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518945B2
Source datasetuspto-grants-2013_08
ORD IDord-9849237030ff48ecb7c9d94bf318f83b
Source noteuspto-grants-2013_08