HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → (S)-3-(3-Bromo-5-methyl-benzylsulfanyl)-2-methyl-propionic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | D-beta-acetylthioisobutyric acid | HCID 2724506 | — |
| Reactant | 1-Bromo-3-(bromomethyl)-5-methylbenzene | HCID 22324261 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (S)-3-(3-Bromo-5-methyl-benzylsulfanyl)-2-methyl-propionic acid | HCID 68541731 | — |
Reaction Steps
A solution of 5.55 g (21 mmol) 1-bromo-3-bromomethyl-5-methyl-benzene and 2.90 ml (21 mmol) (S)-3-acetylsulfanyl-2-methyl-propionic acid in 32 ml methanol is cooled in an ice bath and 4N aqueous sodium hydroxide (15.8 ml, 63 mmol) are added. The reaction mixture is stirred at rt for 3 hrs. EtOAc is added to the mixture and the organic layer is washed with water and brine and evaporated. Filtration over silica gel (flashmaster, hexane to hexane/EtOAc 4/6) gives the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07612055B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-25d74e1d243940ddb7790c5ebb43d38c |
| Source note | uspto-grants-2009_11 |