HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494558Generated: November 1, 2026
1-Bromo-3-methylbutane → HCID 25259505, compound
https://huagongshe.com/reaction/494558
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-3-methylbutane | HCID 7891 | — |
| Reactant | 2-Phenylpropionic acid | HCID 10296 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 25259505 | HCID 25259505 | — |
Reaction Steps
To a solution of lithium bis(trimethylsilyl)amide (278.57 g, 1.66 mol) in tetrahydrofuran (700 mL) was added 2-phenyl propionic acid (100.0 g, 0.666 mol) over 40 minutes maintaining the temperature below 15° C. The solution was warmed 40-45° C. for 20 minutes, then cooled below 25° C. and 1-bromo-3-methylbutane (156.0 g, 1.03 mol) was added. The reaction mixture was heated to 50° C. for 10 h, then was cooled to RT, and concentrated to a thick sludge. Methyl tert-butyl ether (900 mL) and water (1100 mL) were added, and the layers were separated. The organic phase was extracted with H2O (200 mL). The combined aqueous phases were treated with 3 M HCl (520 mL) to adjust the pH to approximately 2. The product was extracted with ethyl acetate (1000 mL) and the organic layer was concentrated to a thick oil to give the title compound. The crude oil (assayed for 136.99 g of Example 39-1, 95.3% assay yield) was used directly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538105B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-a9b863c46284400fb31e24a55f532050 |
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| Source note | uspto-grants-2009_05 |
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