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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985478Generated: October 29, 2026

Sodium hydride → 3-[1,1-bis (Methylethyl)-2-methyl-1-silapropylthio]phenyl acetate

https://huagongshe.com/reaction/985478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantTris(propan-2-yl)silanethiolHCID 3435097—
Reactant3-Iodophenyl acetateHCID 13101769—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product3-[1,1-bis (Methylethyl)-2-methyl-1-silapropylthio]phenyl acetateHCID 1122104552.4%

Reaction Steps

Triisopropylsilanethiol (2.91 ml, 13.5 mmol) was added dropwise to a suspension of sodium hydride (325 mg, 13.5 mmol) in THF (10 ml). After the evolution of hydrogen ceased, a solution of 3-iodophenyl acetate (2.37 g, 9.0 mmol) and tetrakis(triphenylphosphine)palladium (0) (1.04 g, 0.9 mmol) in toluene (90 ml) was added. After refluxing for 16 h under argon, the reaction was cooled to room temperature and the solvent was evaporated under vacuum. The resulting residue was dissolved in ethyl acetate, washed with 1N NaOH and brine, dried with sodium sulfate, filtered, and evaporated under vacuum. The crude product was chomatrographed over silica gel to yield 1.53 g (52%) of 3-[1,1-bis (Methylethyl)-2-methyl-1-silapropylthio]phenyl acetate. NMR 1H Cl3CD δ: 7.34 (m, 2H), 7.23 (t, 1H, J=2.4 Hz), 6.94 (dd, 1H, J=1.2, 8.4 Hz), 2.28 (s, 3H), 1.25 (m, 3H), 1.08 (d, 18 H, J=7.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06872730B2
Source datasetuspto-grants-2005_03
ORD IDord-ff458401309d4f08a5fd876cd4e86c76
Source noteuspto-grants-2005_03