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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362132Generated: October 26, 2026

2-(Dichloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → 2-(1-Chloropropyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

https://huagongshe.com/reaction/362132

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Dichloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 11042041—
ReactantHCID 178418443HCID 178418443—
SolventTetrahydrofuranHCID 8028—
Product2-(1-Chloropropyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 1936464079.8%

Reaction Conditions

Temperature-78 °C

Reaction Steps

2.64 g (12.5 mmol) of 2-(dichloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane were dissolved in 30 ml of tetrahydrofuran and the solution was cooled under a nitrogen atmosphere to -78° C. 11.8 ml (12.5 mmol) of 1.06M ethylmagnesium bromide were added dropwise and the solution was stirred at room temperature for 18 hours. The solution was partitioned between ethyl acetate, saturated sodium chloride solution and 2M hydrochloric acid solution. The aqueous layer was extracted with ethyl acetate and the organic layers were combined and dried over anhydrous sodium sulphate. After filtration and evaporation the oil obtained was distilled to give 2.04 g of 2-[1(RS)-chloropropyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane; b.p. 53° C./0.8 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866684
Source datasetuspto-grants-1999_02
ORD IDord-76325ada409a4ba9a0599450fca9e07d
Source noteuspto-grants-1999_02