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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353274Generated: October 31, 2026

4-Methoxybenzyl alcohol → HCID 18449403, compound

https://huagongshe.com/reaction/2353274

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzyl alcoholHCID 7738—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantSpiro(5-nitroindane)-2,5'-hydantoinHCID 16638331—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18449403HCID 18449403—

Reaction Steps

A mixture of (±)-5′-nitro-spiro[imidazolidine-4,2′-indane]-2,5-dione (1.4 g, 5.66 mmol, described in Intermediate 6), 4-methoxybenzyl alcohol (0.94 g, 6.80 mmol), diethyl azodicarboxylate (1.48 g, 8.49 mmol), and triphenylphosphine (2.23 g, 8.49 mmol) in THF (15 mL) was stirred at ambient temperature for 3 days. The solvent was removed under reduced pressure and the residue was partitioned between saturated aqueous NaHCO3 (15 mL) and CH2Cl2 (50 mL). The organic layer was dried (Na2SO4), filtered, and concentrated under reduced pressure. The crude product was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—90:10 to 60:40, to give the title compound as a yellow solid. MS: m/z=368 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750010B2
Source datasetuspto-grants-2010_07
ORD IDord-d266370b878d4580bc8c3e6b022e640e
Source noteuspto-grants-2010_07