HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorophenol → HCID 68830312, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorophenol | HCID 4684 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | HCID 57592468 | HCID 57592468 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68830312 | HCID 68830312 | — |
Reaction Steps
A solution of [4-(8-methoxy-3-methyl-2,3,4,5-tetrahydro-1-H-3-benzazepine-7-sulfonyl)-phenyl]-methanol D12 (0.12 g), 4-chlorophenol (0.042 g), triphenyl phosphine (0.087 g in tetrahydrofuran (5 mL) was treated with diisopropyl azodicarboxylate (0.066 g). The solution was stirred for 18 hour then the solvent was evaporated and the residue was purified by column chromatography on silica using 0-10% methanol (containing 0.5% aqueous ammonia)-dichloromethane to give the title compound E107, which was converted to the hydrochloride salt. 1H NMR: δ CDCl3 2.36 (3H, s), 2.55 (4H, m), 2.94 (4H, m), 3.73 (3H, s), 5.08 (2H, s) 6.64 (1H, s), 6.87 (2H, d), 7.22 (2H, d), 7.50 (2H, d) 7.84 (1H, s) 7.98 (2H, d). Mass Spectrum MH+ 472
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07504392B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-6705e99bb3be4740825ec1a8e362f849 |
| Source note | uspto-grants-2009_03 |