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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-2-methylpropane | HCID 6555 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 63585886 | HCID 63585886 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 25143957 | HCID 25143957 | 52.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188301B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-cf0ea79ab92f4e62beda5e29e3ffe12e |
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| Source note | uspto-grants-2012_05 |
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