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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842407Generated: October 30, 2026

Tert-butyl 5-[2-(dichloromethyl)-4(rs),5,5-trimethyl-1,3,2-dioxaborolan-4-yl]-3(rs)-methylvalerate → Tert-butyl 5-[2-(1(rs)-chloropropyl)-4(rs),5,5-trimethyl-1,3,2-dioxaborolan-4-yl]-3(rs)-methylvalerate

https://huagongshe.com/reaction/842407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 5-[2-(dichloromethyl)-4(rs),5,5-trimethyl-1,3,2-dioxaborolan-4-yl]-3(rs)-methylvalerateHCID 22619106—
ReactantHCID 178418443HCID 178418443—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 5-[2-(1(rs)-chloropropyl)-4(rs),5,5-trimethyl-1,3,2-dioxaborolan-4-yl]-3(rs)-methylvalerateHCID 22619127100%

Reaction Conditions

Temperature-78 °C

Reaction Steps

0.86 g (2.3 mmol) of tert-butyl 5-[2-(dichloromethyl)-4(RS),5,5-trimethyl-1,3,2-dioxaborolan-4-yl]-3(RS)-methylvalerate was dissolved in 5 ml of tetrahydrofuran and the solution was cooled to −78° C. under a nitrogen atmosphere. 2.6 ml (2.6 mmol) of 1M ethylmagnesium bromide in tetrahydrofuran were added dropwise, the resulting solution was stirred for 16 hours while slowly warming to room temperature and then diluted with ethyl acetate and extracted with 2M hydrochloric acid and brine. The organic phase was dried over sodium sulphate and then evporated under a vacuum to give 0.83 g of tert-butyl 5-[2-(1(RS)-chloropropyl)-4(RS),5 ,5-trimethyl-1,3 ,2-dioxaborolan-4-yl]-3(RS)-methylvalerate as an oil which was used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372883B1
Source datasetuspto-grants-2002_04
ORD IDord-ea12d215b0b14f199e192f4a830bf956
Source noteuspto-grants-2002_04