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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746050Generated: October 27, 2026

Sodium Chloride → 4,4,5,5-Tetramethyl-2-(2-methylbenzo[d][1,3]dioxol-5-yl)-1,3,2-dioxaborolane

https://huagongshe.com/reaction/1746050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5017741—
Reactant5-Bromo-2-methylbenzo[d][1,3]dioxoleHCID 21712592—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product4,4,5,5-Tetramethyl-2-(2-methylbenzo[d][1,3]dioxol-5-yl)-1,3,2-dioxaborolaneHCID 8669983859.3%

Reaction Conditions

Temperature-70 °C

Reaction Steps

5-Bromo-2-methylbenzo[d][1,3]dioxole (1.0 g, 4.7 mmol, prepared as described in Matyus, Peter; Magyar, Kalman; Pihlavista, Marjo; Gyires, Klara; Haider, Norbert; Wang, Yinghua; Woda, Patrick; Dunkel, Petra; Toth-Sarudy, Eva; Turos, Gyoergy, WO2010029379) was dissolved in dry tetrahydrofuran (10 mL), cooled to −70° C. and treated with n-BuLi (2.5 M; 2.1 mL, 4.7 mmol) over 5 min. After 1 h, 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.1 g, 6.0 mmol) was added and the mixture was stirred for 90 min at −70 to −30° C. After addition of saturated NH4Cl (5 mL), the mixture was shaken with ethyl acetate (40 mL) and saturated NaCl (10 mL), dried (Na2SO4) and evaporated. The material was purified by chromatography on silica with a 0-30% ethyl acetate-hexane gradient to give the title compound (730 mg, 59%): 1H NMR (400 MHz, CDCl3) δ 7.33 (dd, J=7.7, 1.1 Hz, 1H), 7.18 (d, J=0.9 Hz, 1H), 6.77 (d, J=7.8 Hz, 1H), 6.25 (q, J=5.0 Hz, 1H), 1.66 (d, J=4.9 Hz, 3H), 1.32 (s, 12H); EIMS m/z 262.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09149038B2
Source datasetuspto-grants-2015_10
ORD IDord-4ad6a2e5c18f464fa31f2640b42e432b
Source noteuspto-grants-2015_10