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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594843Generated: October 26, 2026

Di-tert-butyl [6'-(3-methoxyprop-1-yn-1-yl)dispiro[1,3-oxazole-4,4'-chromene-3',3''-oxetan]-2-yl]imidodicarbonate → Di-tert-butyl [6'-(3-methoxypropyl)dispiro[1,3-oxazole-4,4'-chromene-3',3''-oxetan]-2-yl]imidodicarbonate

https://huagongshe.com/reaction/594843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi-tert-butyl [6'-(3-methoxyprop-1-yn-1-yl)dispiro[1,3-oxazole-4,4'-chromene-3',3''-oxetan]-2-yl]imidodicarbonateHCID 86724253—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductDi-tert-butyl [6'-(3-methoxypropyl)dispiro[1,3-oxazole-4,4'-chromene-3',3''-oxetan]-2-yl]imidodicarbonateHCID 8672422599.9%

Reaction Steps

A mixture of di-tert-butyl[6′-(3-methoxyprop-1-yn-1-yl)dispiro[1,3-oxazole-4,4′-chromene-3′,3″-oxetan]-2-yl]imidodicarbonate (34.7 mg, 0.067 mmol) and 10% palladium on carbon (7 mg) in EtOH (1.4 mL) was stirred for 13 hours under a hydrogen atmosphere (4.5 kgf/cm2). The mixture was filtered off, and the filtrate was evaporated to give crude di-tert-butyl [6′-(3-methoxypropyl)dispiro[1,3-oxazole-4,4′-chromene-3′,3″-oxetan]-2-yl]imidodicarbonate (34.7 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242973B2
Source datasetuspto-grants-2016_01
ORD IDord-f74b704473414cf2a9ac478408a6ae88
Source noteuspto-grants-2016_01