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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362134Generated: October 26, 2026

2-(Dichloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → 2-[1(RS)-chlorobutyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

https://huagongshe.com/reaction/362134

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Dichloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 11042041—
ReactantHCID 178455851HCID 178455851—
SolventTetrahydrofuranHCID 8028—
Product2-[1(RS)-chlorobutyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 1936467773.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

0.5 g (2.37 mmol) of 2-(dichloromethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane was dissolved in 10 ml of tetrahydrofuran and the solution was cooled under a nitrogen atmosphere to -78° C. 2.4 ml (2.4 mmol) of 1M propylmagnesium 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 evaporation there was obtained 0.38 g of 2-[1(RS)-chlorobutyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane as an oil which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866684
Source datasetuspto-grants-1999_02
ORD IDord-96ddd13dce0d48249ea5d25bd1dd9b22
Source noteuspto-grants-1999_02