HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650547Generated: October 30, 2026
Bromomethyl 4-methoxyphenyl ketone → HCID 12330847, compound
https://huagongshe.com/reaction/650547
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromomethyl 4-methoxyphenyl ketone | HCID 4965 | — |
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12330847 | HCID 12330847 | 81.6% |
Reaction Steps
Potassium thioacetate (2.28 g, 20 mmol) was added to a solution of 2-bromo-4′-methoxy acetophenone (4.58 g, 20 mmol) in absolute ethanol (150 ml). the reaction was stirred at ambient temperature under nitrogen for 16 hours at which time the white precipitate that had formed was filtered and the ethanol removed at reduced pressure. The residue was dissolved in dichloromethane (250 ml) and washed with water (200 ml), brine (200 ml), dried over Na2SO4 and the solvent removed at reduced pressure. The resulting residue was chromatographed on silica with a gradient from 10%-35% ethyl acetate in hexane to yield 3.4 g (76%) of 2-thioacetyl-4′-methoxy acetophenone. 1H NMR (CDCl3) δ 2.36 p (s, 3h), 3.84 (s, 3h), 4.33 (s, 2h), 6.9 (d, 2h, J=9.2 Hz), 7.9 (d, 2h, J=9.2 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06274590B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-be6e7a03abdb47848a1b011e62e1e366 |
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| Source note | uspto-grants-2001_08 |
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