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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362142Generated: 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/362142

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 1 M ethylmagnesium bromide in tetrahydrofuran were added dropwise, the resulting solution wasstirred 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 evporatedunder 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 numberUS05866684
Source datasetuspto-grants-1999_02
ORD IDord-ba523794496146a7b2207d7a97ddb400
Source noteuspto-grants-1999_02