HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Methyl 4-benzyloxy-3-tert-butyl-5-iodobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 3-t-butyl-4-hydroxy-5-iodobenzoate | HCID 12084815 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 4-benzyloxy-3-tert-butyl-5-iodobenzoate | HCID 12084816 | 80% |
Reaction Steps
24.1 g (72 mmol) of methyl 3-tert-butyl-4-hydroxy-5-iodobenzoate are dissolved in 200 mL of dimethylformamide. 3.47 g (86 mmol) of 60% sodium hydride are added slowly and the reaction medium is stirred for 1 hour. 9.4 mL (79 mmol) of benzyl bromide are then added and the medium is stirred at room temperature for 2 hours, and is then hydrolysed and extracted with ethyl ether. The organic phase is washed 3 times with water and then concentrated under reduced pressure. The residue is purified by chromatography (eluent: 98 heptane/2 ethyl acetate). A yellow oil is obtained (m=24.3 g; yield=80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07468457B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-b74b099914ac49539d1ba15387f66d1b |
| Source note | uspto-grants-2008_12 |