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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931834Generated: November 3, 2026

1-Bromo-2-methylpropane → HCID 25143957, compound

https://huagongshe.com/reaction/1931834

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-methylpropaneHCID 6555—
ReactantSodium CarbonateHCID 10340—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 63585886HCID 63585886—
SolventAcetonitrileHCID 6342—
ProductHCID 25143957HCID 2514395752.1%

Reaction Steps

In a sealed tube a mixture of enantiomer E2 of 3-(3,5-difluorophenyl)pyrrolidin-3-ol (0.28 g, 1.45 mmol), acetonitrile (15 mL), potassium carbonate (0.4 g, 2.9 mmol) and 1-bromo-2-methylpropane (0.15 mL, 1.59 mmol) was stirred at ambient temperature for 5 h and then at 60° C. for 2 h. Aqueous sodium carbonate (10%, 5 mL) was added and the aqueous phase was extracted with ethyl acetate (2×50 mL). The combined organic phase was dried (Na2SO4) and evaporated. Purification by flash chromatography on silica gel (ethyl acetate/methanol, 10:1) gave the title compound (0.193 g). [α]D=−22.9° (methanol). The amine was converted to the oxalic acid salt and recrystallized from ethanol/diisopropyl ether: M.p. 162-163° C.; MS m/z (relative intensity, 70 eV) 255 (M+, 2), 212 (bp), 182 (46), 213 (13), 57 (10), 127 (10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188301B2
Source datasetuspto-grants-2012_05
ORD IDord-cf0ea79ab92f4e62beda5e29e3ffe12e
Source noteuspto-grants-2012_05