HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118388Generated: October 30, 2026
Triisopropyl phosphite → HCID 68877610, compound
https://huagongshe.com/reaction/2118388
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triisopropyl phosphite | HCID 8304 | — |
| Reactant | 2-(Trimethylsilylmethyl)allyl acetate | HCID 4428347 | — |
| Reactant | HCID 12083970 | HCID 12083970 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68877610 | HCID 68877610 | — |
Reaction Steps
To a solution of 6-methoxymethoxy coumarin 17a (21 g, 0.102 mol) and Pd(OAc)2 (2.75 g, 0.012 mol) in 500 mL THF add 2-(acetoxymethyl)allyl-trimethylsilane (26 mL, 0.122 mol) followed by triisopropyl phosphite (18.1 mL, 0.073 mol). After stirring at 60° C. overnight, cool the solution to RT, concentrate under reduced pressure, and dilute with EtOAc. Wash the solution with saturated aqueous sodium bicarbonate and brine. Dry over Na2SO4, and then concentrate to an oil. Purify the material by silica gel chromatography (Biotage 40M+65M columns, 10 to 30% EtOAc/Hex over 60 min at 50 mL/min followed by 30 to 50% EtOAc/Hex over 60 min at 50 mL/min) to give 18.3 g (0.070 mol, 69%) of cyclopentanoid 18 and 3.8 g (18.3 mmol, 18%) of recovered starting material. HRMS(ES+) calc for C15H17O4: 261.1127, found: 261.1122 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07442812B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-c35bed69faf142a2bd54fc1d40de5739 |
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| Source note | uspto-grants-2008_10 |
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