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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Tris(propan-2-yl)silanethiol | HCID 3435097 | — |
| Reactant | 3-Iodophenyl acetate | HCID 13101769 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[1,1-bis (Methylethyl)-2-methyl-1-silapropylthio]phenyl acetate | HCID 11221045 | 52.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06872730B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-ff458401309d4f08a5fd876cd4e86c76 |
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| Source note | uspto-grants-2005_03 |
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