HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 66756606, compound → HCID 66757012, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 66756606 | HCID 66756606 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 66757012 | HCID 66757012 | — |
Reaction Steps
2-(3-Benzyloxy-4-nitrophenyl)-malonic acid tert-butyl ester ethyl ester (5.00 g, 12.0 mmol) is suspended in formic acid (60 mL) and stirred at RT for 18 h. The solvent is removed under reduced pressure and the residue taken up in EtOAc (100 mL). The organic solution is extracted with saturated NaHCO3 (2×50 mL) and brine (30 mL), before being dried over Na2SO4 and concentrated to an oil. Purification by flash column (10-15% EtOAc/hexanes) affords (3-benzyloxy-4-nitrophenyl)-acetic acid ethyl ester as a yellow oil: MS (M+H)+=316.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119666B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-23d49581e8ab4173bcc0c0733c756f0c |
| Source note | uspto-grants-2012_02 |