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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667544Generated: October 29, 2026

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

https://huagongshe.com/reaction/1667544

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) for 20 min. 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 min. 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 numberUS08044216B2
Source datasetuspto-grants-2011_10
ORD IDord-196a754c66794b62a394bfe11e9594da
Source noteuspto-grants-2011_10