HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207193Generated: November 2, 2026
Hydrochloric Acid → HCID 118557958, compound
https://huagongshe.com/reaction/2207193
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Stannane, tributyl(1-ethoxyethenyl)- | HCID 619414 | — |
| Reactant | HCID 118558042 | HCID 118558042 | — |
| Catalyst | Triphenylphosphine | HCID 11776 | — |
| Catalyst | (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium | HCID 6505921 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 118557958 | HCID 118557958 | 81% |
Reaction Steps
A toluene solution (3 mL) of compound 89 (0.4 g, 1.1 mmol), Pd(dba)2 (25.3 mg, 0.044 mmol) and PPh3 (23.1 mg, 0.088 mmol) was stirred at room temperature under argon for 15 min. Then, (1-ethoxyvinyl)tri(n-butyl)stannane (0.38 mL, 1.1 mmol) in toluene (3 mL) was added and the resulting mixture was stirred overnight at 110° C., cooled to room temperature and filtered on Celite, washed with EtOAc and concentrated under reduced pressure. Purification on silica gel (gradient of EtOAc in Petroleum ether) afford the product which was placed in presence of an aqueous solution of HCl 1M for 30 minutes at room temperature. After neutralization with a saturated aqueous solution of NaHCO3, aqueous phase was extracted with dichloromethane and the combined organic layers were dried over magnesium sulfate to afford the title compound 97 (Yield 288.1 mg, 81%) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376387B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-02f35757922f4044bc68eb9d6b31c0c4 |
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| Source note | uspto-grants-2016_06 |
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