HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 2-(1-Methylcyclohexyl)-4-bromoanisole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-Bromophenol | HCID 7808 | — |
| Reactant | 1-Methylcyclohexanol | HCID 11550 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 2-(1-Methylcyclohexyl)-4-bromoanisole | HCID 10684359 | 13% |
Reaction Steps
A mixture of 1-methylcyclohexanol (100.00 g, 0.876 mol) and 4-bromophenol (101.01 g, 0.584 mol) in CH2Cl2 (1.0 L) and H2SO4 (44 mL) was heated to reflux for 4 days. The mixture was cooled to RT. The reaction was poured in a separatory funnel and washed with water, 0.5 N NaHCO3 (till neutralized), brine and dried (MgSO4). The mixture was filtered, evaporated and the residue was purified on silica gel (eluant: hexane: CH2Cl2, 4:1) to give a total amount of 2-(1-methylcyclohexyl)-4-bromoanisole as an oil (29.70 g, 13%). 1H NMR (300 MHz, CDCl3): δ 1.30 (s, 3H), 1.30–1.70 (m, 8 H), 2.00–2.15 (m, 2H), 4.87 (s, 1H), 6.54 (d, J=8.4 Hz, 1H), 7.15 (dd, J1=8.4 Hz, J2=2.4 Hz, 1H), 7.36 (d, J=2.4 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07153875B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-84d2133b76a14975a4f125ee41a8d61e |
| Source note | uspto-grants-2006_12 |