HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → HCID 23433529, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 23433604 | HCID 23433604 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23433529 | HCID 23433529 | — |
Reaction Steps
To a solution of N-tert-butyloxycarbonyl-1,2-dihydro-2,2-dimethyl-4-hydroxymethyl-6-phenylquinoline (structure 11, where R1 =phenyl) (230 mg, 0.630 mmol) and carbon tetrabromide (220 mg, 0.662 mmol) in 5 mL of dichloromethane at 0° C. was added triphenylphosphine (174 mg, 0.662 mmol) in 2 mL of dichloromethane. The reaction mixture was allowed to warm to rt and stirred for 1 h. The mixture was concentrated in vacuo to a residue that was subjected to flash chromatography (silica gel, hexane/ethyl acetate, 9:1) to give structure 12, where R1 =phenyl (72 mg, 27%). 1H NMR (acetone d6) 7.67 (m, 3H), 7.52 (dd,J=8.7, 2.1, 1H), 7.45 (t, 2H), 7.32 (m, 2H), 6.07 (s, 1H), 4.60 (s, 2H), 1.55 (s, 6H), 1.53 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06093821 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-f38c0b23b1a0472cadaf5516ac82e01d |
| Source note | uspto-grants-2000_07 |