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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873706Generated: October 30, 2026

Hydrochloric Acid → HCID 86724248, compound

https://huagongshe.com/reaction/873706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
ReactantHCID 86724230HCID 86724230—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
SolventMethanolHCID 887—
ProductHCID 86724248HCID 8672424875.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of di-tert-butyl (6′-bromodispiro[cyclopropane-1,3′-chromene-4′,4″-[1,3]oxazol]-2″-yl)imidodicarbonate (200 mg, 0.393 mmol), bis(dibenzylideneacetone)palladium (0) (22.6 mg, 0.039 mmol), and tri-tert-butylphosphonium tetrafluoroborate (11.6 mg, 0.039 mmol) was added lithium bis(trimethylsilyl)amide (1 M in toluene, 1.96 mL, 1.96 mmol) at ambient temperature. After stirring for 1 hour at 100° C., the mixture was cooled down to ambient temperature. To the mixture were added 1M aqueous HCl (1.96 mL) and MeOH (1.96 mL) at ambient temperature, and the mixture was stirred for 30 minutes at the same temperature. The mixture was extracted with CHCl3, and the organic layer was dried over Na2SO4 and filtered. The filtrate was concentrated at reduced pressure and purified with column chromatography on silica gel (hexane-EtOAc, a linear gradient of EtOAc from 0 to 90%) to afford tert-butyl (6′-aminodispiro[cyclopropane-1,3′-chromene-4′,4″-[1,3]oxazol]-2″-yl)carbamate (103 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975415B2
Source datasetuspto-grants-2015_03
ORD IDord-4de3b76a78e9453faf1569d3c2da1641
Source noteuspto-grants-2015_03