HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689466Generated: October 31, 2026
Ethyl isobutyrate → Ethyl 7-bromo-2,2-dimethylheptanoate
https://huagongshe.com/reaction/1689466
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl isobutyrate | HCID 7342 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 1,5-Dibromopentane | HCID 8100 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 7-bromo-2,2-dimethylheptanoate | HCID 11265571 | — |
Reaction Steps
To a solution of diisopropylamine (5.82 mL) in THF (30 mL) was added n-butyllithium (2.5M in hexanes, 16.4 mL) at 0° C. and the mixture was stirred for 30 min at this temperature before being cooled to −78° C. Ethyl isobutyrate (5 mL) was added dropwise and the resultant mixture was stirred at −78° C. for 1 h before addition of 1,5-dibromopentane (5.61 mL). The reaction mixture was stirred at −78° C. for 1 h then at RT for 2.5 h before being poured into saturated ammonium chloride solution. The solution was extracted with ethyl acetate (×2), then the combined organics were washed with water and dried over sodium sulphate, filtered and evaporated in vacuo. Purification was by silica gel chromatography eluting with 0-25% ethyl acetate in cyclohexane to give the subtitled compound as a yellow liquid. Yield 4.45 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08148373B2 |
|---|
| Source dataset | uspto-grants-2012_04 |
|---|
| ORD ID | ord-3725100818c848f5b7c673f9262bc886 |
|---|
| Source note | uspto-grants-2012_04 |
|---|