Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705193Generated: October 29, 2026

2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → HCID 66652582, compound

https://huagongshe.com/reaction/705193

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5017741—
ReactantHCID 66654962HCID 66654962—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66652582HCID 66652582—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 1,3-difluoro-5-(2-methoxyethoxyl)benzene (1.0 eq) in dry THF (0.2M) under an atmosphere of N2 at −78° C. was added n-butyllithium (1 eq, 1.6M in hexanes) slowly keeping the internal temperature below −65° C. The reaction was stirred for 1 hr at −78° C., followed by the addition of 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (2.1 eq). The reaction was allowed to warm to room temperature. Upon completion, the reaction was quenched with NaHCO3 (sat) and extracted with EtOAc. The organics were washed with brine, dried over Na2SO4, filtered and concentrated to yield 2-(2,6-difluoro-4-(2-methoxyethoxyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolαne. 1H NMR (400 MHz, <cdcl3>) δ ppm 6.42 (d, 2 H), 4.10 (m, 2H), 3.74 (m, 2H), 3.44 (s, 3 H), 1.37 (s, 12 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09173883B2
Source datasetuspto-grants-2015_11
ORD IDord-107636c4e55d4a85874f89712699a88c
Source noteuspto-grants-2015_11