HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873706Generated: October 30, 2026
Hydrochloric Acid → HCID 86724248, compound
https://huagongshe.com/reaction/873706
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | Tri-tert-butylphosphine tetrafluoroborate | HCID 2734635 | — |
| Reactant | HCID 86724230 | HCID 86724230 | — |
| Catalyst | (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium | HCID 6505921 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86724248 | HCID 86724248 | 75.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975415B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-4de3b76a78e9453faf1569d3c2da1641 |
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| Source note | uspto-grants-2015_03 |
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