HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → (S)-2-tert-butoxycarbonylamino-4-phenoxy-butyric acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | Methyl N-(tert-butoxycarbonyl)-L-homoserinate | HCID 10561607 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-2-tert-butoxycarbonylamino-4-phenoxy-butyric acid methyl ester | HCID 67178164 | 61.2% |
Reaction Steps
To a stirred solution of (S)-(tert-butoxycarbonylamino)-4-hydroxybutyric acid methyl ester (1.43 g; CAS 120042-11-7) in THF (4 ml) were added phenol (692 mg), triphenylphosphine (1.77 g) and diisopropyl azodicarboxylate (1.36 g). The resulting yellow solution was stirred at room temperature overnight. The reaction mixture was evaporated and purified by column chromatography (SiO2; gradient: heptane/EtOAc 100:0→90:10) to give (S)-2-tert-butoxycarbonylamino-4-phenoxy-butyric acid methyl ester (1.16 g, 61%) as a light yellow oil. MS (ISP): 210.1 ([M+H-BOC]+)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08242153B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-d88fb28ac194438da3f0b27f349a0745 |
| Source note | uspto-grants-2012_08 |