HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394628Generated: November 2, 2026
4'-Fluoroacetophenone → HCID 16741950, compound
https://huagongshe.com/reaction/1394628
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4'-Fluoroacetophenone | HCID 9828 | — |
| Reactant | Methyl Thioglycolate | HCID 16907 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 16741950 | HCID 16741950 | — |
Reaction Steps
Methyl thioglycolate was dissolved in DMF (10 ml) and this mixture was cooled to 0° C. under an atmosphere of nitrogen. NaH (750 mg of 60% mineral oil dispersion, 18.1 mmol) was then added in one portion. After 5 min., the ice bath was removed and p-fluoroacetophenone (1 ml, 8.2 mmol) was added in one portion. The reaction mixture stirred at ambient temperature for 1 hr then diluted with ethyl acetate (50 ml) and washed with water. The aqueous layer was extracted with ethyl acetate (2×50 ml) and the combined organics dried over MgSO4 and concentrated in vacuo to yield (4-acetyl-phenylsulfanyl)-acetic acid methyl ester, as a white waxy solid (1.48 g, 80%). 1H NMR (250 MHz, CDCl3): δ 7.80 (d, 2H, J=9.4), 7.32 (d, 2H, J=9.4), 3.71 (s, 2H), 3.67 (s, 3H), 2.50 (s, 3H). MS [EI+] 225 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07348359B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-62fac8616bc94344a1c1dff01de24a76 |
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| Source note | uspto-grants-2008_03 |
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