HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromobenzyl bromide → HCID 59749687, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromobenzyl bromide | HCID 76965 | — |
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 59749687 | HCID 59749687 | — |
Reaction Steps
To a solution of 2-bromo-benzyl bromide (1 ml, Aldrich 187070) in acetone was added potassium thioacetate (0.9 g, Aldrich 241776) and the mixture refluxed for 2 hr. The reaction mixture was purified on a plug of silica eluting through with further acetone to give thioacetic acid S-(2-bromo-benzyl) ester (1.57 g) 1H-NMR (400 MHz, CDCl3): 2.34 (3H, s), 4.24 (2H, s), 7.09-7.14 (1H, dt), 7.23-7.27 (1H, dt), 7.44-7.46 (1H, dd), 7.54-7.56 (1H, dd).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08569301B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-70238789d79b458b97f7ca56c30cf795 |
| Source note | uspto-grants-2013_10 |