HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-[4-(Heptyloxy)phenyl]ethanone → 2-Bromo-1-(4-(heptyloxy)phenyl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-[4-(Heptyloxy)phenyl]ethanone | HCID 577944 | — |
| Reactant | Phenyltrimethylammonium bromide dibromide | HCID 17977687 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Bromo-1-(4-(heptyloxy)phenyl)ethanone | HCID 53909186 | 137.7% |
Reaction Steps
To a stirring solution of 1-(4-(heptyloxy)phenyl)ethanone (500 mg, 2.13 mmol) in THF (8.5 mL) under nitrogen was added phenyltrimethylammonium tribromide (842 mg, 2.24 mmol). The reaction mixture was stirred at room temperature for 2 h, filtered under vacuum and the captured solid washed with THF. The combined liquors were concentrated to afford 919 mg (100%) of 2-bromo-1-(4-(heptyloxy)phenyl)ethanone INT-4 as a yellow oil. LCMS-ESI (m/z) calculated for C15H21BrO2: 313.2. found 313.0 [M+H]+, tR=2.12 min. (Method 4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09260427B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-9a510abdb0314579b73403b34990b8fa |
| Source note | uspto-grants-2016_02 |