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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844075Generated: October 31, 2026

Allyltributylstannane → HCID 10976292, compound

https://huagongshe.com/reaction/1844075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyltributylstannaneHCID 90628—
ReactantMethyl 2-(2-iodophenyl)acetateHCID 640185—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 10976292HCID 1097629265%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a solution of methyl 2-iodophenylacetate (1.00 g, 3.62 mmol, prepared from the corresponding acid according to litt. Tetrahedron 63, 2007, 9979) in toluene (45 mL) was added Tetrakis(triphenylphosphine)palladium (209 mg, 0.0.181 mmol) and allyl tributylstannane (1.35 mL, 4.34 mmol). The resulting solution was heated to 110° C. for 20 h and then cooled down. The solvents were removed in vacuo. The yellow oil was partitioned between acetonitrile (30 mL) and hexane (30 mL) and the acetonitrile layer was washed with hexane (2*30 mL). The acetonitrile was removed in vacuo and the residue was purified by flash chromatography eluting with cyclohexane and ethyl acetate (15/1) to give Methyl 2-allylphenylacetate (colourless oil, 446 mg, 65%). C12H14O2; MW: 190.24; LCMS (method A) RT 1.74 min; ES: 191 (100%, MH+); IR. 2951, 1734 cm−1; 1H NMR (400 MHz, CDCl3) δ 7.14-7.41 (4H, m), 5.99 (1H, m), 5.12 (1H, m), 5.03 (1H, m), 3.73 (3H, s), 3.72 (2H, s), 3.47 (2H, dt) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946280B2
Source datasetuspto-grants-2015_02
ORD IDord-f58ad7c66031475eacbc5f4d5fd0b176
Source noteuspto-grants-2015_02