Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Isobutylene | HCID 8255 | — |
| Reactant | (2R)-2-bromo-4-methylpentanoic acid | HCID 12697060 | — |
| Reactant | HCID 86583683 | HCID 86583683 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53857518 | HCID 53857518 | — |
Reaction Steps
Into dichloromethane (80 mL) was condensed isobutene to double the volume (at -50° C. CHCl3 /dry ice). To this solution was added (2R)-2-bromo-4-methylpentanoic acid (28 g, 143.6 mmol) and maintaining the temperature between -40° and -50° C. concentrated sulphuric acid (1 mL) was added dropwise. The reaction was then allowed to warm to room temperature over 20 hours. The solution was then concentrated before adding additional methylene chloride (300 mL) which was subsequently washed with saturated NaHCO3 (2×100 mL) followed by water (2×100 mL). After drying over Na2SO4, the organic layer was filtered and concentrated to give a yellow oil. The material was distilled to give 23 g of (2R)-2-bromo-4-methylpentanoic acid t-butyl ester as a clear colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05773428 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-bb934fb5922a41449005224af99f8d16 |
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| Source note | uspto-grants-1998_06 |
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