HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → HCID 21077868, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 84046672 | HCID 84046672 | — |
| Product | HCID 21077868 | HCID 21077868 | 84% |
Reaction Steps
A solution of diethyl azodicarboxylate (0.74 ml, 4.7 mmol) in anhydrous dichloromethane (3 ml) was added to a stirred, ice-methanol cooled solution of (RS)-1-tert-butoxycarbonyl)-2-(2-hydroxyethyl)-4-methoxycarbonylpiperazine (D7) (1.35 g, 4.69 mmol), phenol (0.441 g, 4.69 mmol) and triphenylphosphine (1.23 g, 4.69 mmol) in anhydrous dichloromethane (40 ml). The mixture was stirred at room temperature for 18 h then evaporated in vacuo. The residue was chromatographed on silica gel eluting with 10–20% ethyl acetate in hexane to give the title compound (1.43 g, 84%). 1H NMR (CDCl3) δ: 1.38 (9H, m), 1.85–2.20 (2H, m), 2.75–3.20(3H, m), 3.72 (3H, s), 3.80–4.20 (5H, m), 4.39 (1H, broad m), 6.75–7.00 (3H, m), 7.15–7.35 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07166608B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-b821133172754d2695b46481f667ed69 |
| Source note | uspto-grants-2007_01 |