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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390889Generated: October 29, 2026

Pinacol → 2-(Chloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

https://huagongshe.com/reaction/2390889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPinacolHCID 6425—
ReactantChloroiodomethaneHCID 11644—
ReactantTriisopropyl borateHCID 21531—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2-(Chloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 1112681081%

Reaction Steps

To the mixture of triisopropyl borate (15 ml, 65 mmol), chloroiodomethane (13 g, 72 mmol), and tetrahydrofuran (78 ml), n-butyllithium (a 1.6 M n-hexane solution, 41 ml, 65 mmol) was added dropwise at −78° C. (an outer temperature) over 20 minutes, and then the obtained mixture was stirred at room temperature for 2.5 hours. The reaction mixture was cooled to 0° C. (an outer temperature), and a 4 N hydrochloric acid-ethyl acetate solution was added dropwise thereto at the same temperature until the reaction mixture became neutral. At the same temperature, pinacol (7.7 g, 65 mmol) was added to the reaction mixture, and then the reaction mixture was stirred at room temperature for 40 minutes. The solvents were evaporated under reduced pressure, and then the obtained residue was distilled under reduced pressure (63-70° C., 11 mmHg), thereby obtaining the entitled compound (9.2 g, 52 mmol, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273885B2
Source datasetuspto-grants-2012_09
ORD IDord-61095631ca8f4d5986f391df5efc7432
Source noteuspto-grants-2012_09