HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553591Generated: October 26, 2026
Sodium Methoxide → HCID 59267977, compound
https://huagongshe.com/reaction/553591
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Ethyl 2-(acetylthio)-2-methylpropanoate | HCID 57937863 | — |
| Reactant | 2-(tetrahydro-2H-pyran-4-yl)ethyl 4-methylbenzenesulfonate | HCID 59267964 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59267977 | HCID 59267977 | 108.9% |
Reaction Steps
To a solution of 1.9 g (6.7 mmol) of toluene-4-sulfonic acid 2-(tetrahydro-pyran-4-yl)-ethyl ester in ethanol (20 mL) are added 1.4 g (26.8 mmol) of sodium methoxide, followed by 1.27 g (6.7 mmol) of 2-acetylsulfanyl-2-methyl-propionic acid ethyl ester. The reaction mixture is heated in a microwave at 130° C. for 0.5 h. The solvent is removed under reduced pressure. The residue is partitioned between saturated aqueous NaHCO3 solution (25 mL) and DCM (25 mL). The layers are separated and the aqueous phase extracted with DCM (2×25 mL). The combined organic extracts are dried over Na2SO4, filtered and the solvent is removed under reduced pressure to afford 1.9 g of 2-methyl-2-[2-(tetrahydro-pyran-4-yl)-ethylsulfanyl]-propionic acid ethyl ester. Yield: 100%; ES-MS: m/z 261 [M+H]; 1H NMR (250 MHz, CHLOROFORM-d) δ ppm 1.15-1.38 (5H, m), 1.42-1.70 (12H, m), 2.59-2.71 (1H, m), 3.37 (2H, td, J=11.73, 1.98 Hz), 3.95 (2H, ddd, J=11.04, 3.88, 0.91 Hz), 4.18 (2H, q, J=7.16 Hz)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08048899B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-ac471472dbad440d83c5e1f4992dcd21 |
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| Source note | uspto-grants-2011_11 |
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