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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642630Generated: November 2, 2026

HCID 66756606, compound → HCID 66757012, compound

https://huagongshe.com/reaction/1642630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66756606HCID 66756606—
SolventFormic AcidHCID 284—
ProductHCID 66757012HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119666B2
Source datasetuspto-grants-2012_02
ORD IDord-23d49581e8ab4173bcc0c0733c756f0c
Source noteuspto-grants-2012_02