HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → Methyl 2-(3-tert-Butoxycarbonylaminopropoxy)-4-tert-butylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | tert-butyl N-(3-bromopropyl)carbamate | HCID 4460490 | — |
| Reactant | Methyl 4-tert-butyl-2-hydroxybenzoate | HCID 20777194 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-(3-tert-Butoxycarbonylaminopropoxy)-4-tert-butylbenzoate | HCID 68530190 | 45.2% |
Reaction Steps
Methyl 4-tert-butyl-2-hydroxybenzoate (2.41 g, 11.6 mmol) was dissolved in DMF (15 mL) and K2 CO3 (2.39 g, 17.4 mmol) and N-Boc-3-bromopropylamine (4.14 g, 17.4 mmol) was added using DMF (10 mL) to aid the transfer. Potassium iodide (0.30 g) was added, and the reaction stirred at room temperature under nitrogen for 18 hr. The DMF was removed in vacuo and the residue taken up in ethyl acetate and washed with water and brine, dried, and the solvent removed in vacuo to give a viscous brown oil. Purification by chromaotgraphy over silica on a preparative scale apparatus, eluting with a gradient of hexane to hexane:ethyl acetate (70:30) gave 1.91 g (45.2%) of a viscous yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700628B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-77670657196546109d8e761506ef5c33 |
| Source note | uspto-grants-2010_04 |