HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 22719690, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 2-[(Acetylthio)methyl]-4-methylpentanoic acid | HCID 13017557 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22719690 | HCID 22719690 | 83.2% |
Reaction Steps
A solution of 3-acetylthio-2-isobutylpropionic acid [obtained by Michael addition of thiolacetic acid onto 2-isobutylacrylic acid] (7 g, 34.3 mmol), benzyl bromide (4.29 ml, 36 mmol) and DBU (5.2 ml, 35 mmol) in toluene (55 ml) was stirred for 18 hours at room temperature. The solvents were evaporated in vacuo. The residue was partitioned between ethyl acetate and 5% sodium bicarbonate. The organic layer was washed with brine and dried over MgSO4. Purification of the residue by chromatography on silica gel (eluant: dichloromethane-ether (9:1)) gave benzyl 3-acetylthio-2-isobutylpropionate (8.4 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07342020B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-03df5bb379af4589bd211cc3f34c3e31 |
| Source note | uspto-grants-2008_03 |