HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromobenzyl bromide → HCID 18977582, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Reactant | 2-Cyclohexenone, 5,5-dimethyl- | HCID 138322 | — |
| Reactant | HCID 10593144 | HCID 10593144 | — |
| Product | HCID 18977582 | HCID 18977582 | — |
Reaction Steps
This compound was prepared from 5,5-dimethylcyclohex-2-en-1-one (8) and p-bromobenzyl bromide in three steps in the manner described for the synthesis of olefin (13). 1H NMR (400 MHz, CDCl3) δ 0.94 and 0.97 (2s, 2×3H, geminal-CH3 's), 2.62 and 2.82 (d of ABq, 2H, benzylic-CH2), 4.25 and 4.61 (2s, 2×1H, methylidene-CH2), 6.98 (d, 2H, Ar--H), 7.34 ppm (d, 2H, Ar--H). [This compound is also referred to as Compound "O" or 120130]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05808139 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-f8b972d3a8df422a9b2adfdba86ec417 |
| Source note | uspto-grants-1998_09 |