HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21996962, compound → HCID 70149291, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21996962 | HCID 21996962 | — |
| Reactant | HCID 21996984 | HCID 21996984 | — |
| Product | HCID 70149291 | HCID 70149291 | — |
Reaction Steps
Employing the same general procedure as for the preparation of 4-bromo-1-isopropoxy-2-[(1-p-tolyl)vinyl]benzene (Compound S), 81.5 mg (0.3 mmol) of 4-bromo-2-[(1-m-tolyl)vinyl]phenol (Compound N) was converted into the title compound using 164 mg (0.6 mmol) of triphenylphosphine, 0.10 mL (108 mg, 0.6 mmol) of diethylazodicarboxylate, 0.05 mL (39 mg, 0.6 mmol) of isopropanol and 3 mL of tetrahydrofuran. The reaction was sluggish necessitating addition (after 23 hours of stirring at ambient temperature) of another equivalent of reagents (initially only ½ of the above amounts were added) and stirring for 4 additional days. Purification by flash chromatography (silica, 10% ethyl acetate in hexane) gave the title compound as a pink oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06235923B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-a1a36f0b352945de880039486e0cac17 |
| Source note | uspto-grants-2001_05 |