HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420277Generated: October 31, 2026
Triphenylphosphine → HCID 131729366, compound
https://huagongshe.com/reaction/420277
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Reactant | HCID 66649728 | HCID 66649728 | — |
| Product | HCID 131729366 | HCID 131729366 | — |
Reaction Steps
A solution of (3aR*,7S*,7aS*)-7-(4-amino-3-fluoro-5-vinyl-benzyl)-3-(3-tert-butyl-benzyl)-5,5-dioxo-hexahydro-1-oxa-5lambda*6*-thia-3-aza-inden-2-one (0.215 g, 0.44 mmol) in CH2Cl2-MeOH 4:1 (10 mL) was ozonized at −78° C. until the educt disappeared. After addition of PPh3 (0.139 g, 0.53 mmol) the reaction mixture was allowed to warm to 25° C. and the solvents were removed under reduced pressure. The title compound was obtained after flash-chromatography on silica gel (hexane-EtOAc 2:1) as white solid: ESIMS [M−H]−=487.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093406B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-8a263ad329ed46f4b73c026d3ba94df4 |
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| Source note | uspto-grants-2012_01 |
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