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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899433Generated: October 28, 2026

Triisopropyl phosphite → HCID 67076954, compound

https://huagongshe.com/reaction/899433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl phosphiteHCID 8304—
Reactant2-(Trimethylsilylmethyl)allyl acetateHCID 4428347—
ReactantHCID 59685168HCID 59685168—
Catalystpalladium(II) acetateHCID 167845—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67076954HCID 67076954—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of preparation 4 (198 mg, 0.64 mmol) and Pd(OAc)2 (17 mg, 0.076 mmol) in 4 mL THF add 2-(acetoxymethyl)allyl-trimethylsilane (0.163 mL, 0.122 mmol) followed by triisopropyl phosphite (0.12 mL, 0.49 mmol). After stirring at 60° C. overnight, cool the solution to room temperature, 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 (10 g, 10 to 30% EtOAc/Hex over 30 min at 35 mL/min) to give 80 mg (0.208 mol, 63%) of preparation 6 and 30 mg (0.091 mmol, 27%) of recovered starting material. 1H NMR (400 MHz, CDCl3) δ 7.48-7.36 (m, 6H), 7.01 (d, 1H, J=3.1 Hz), 5.10 (s, 2H), 5.01 (m, 2H), 3.97 (s, 3H), 3.43 (dt, 1H, J=7.5, 3.1 Hz), 3.21-3.10 (m, 2H), 2.86-2.74 (m, 2H), 2.43 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07354951B2
Source datasetuspto-grants-2008_04
ORD IDord-af9dbffe209e483e85d2a3b4c7caaf86
Source noteuspto-grants-2008_04