HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030001Generated: October 26, 2026
Benzene → 2-Methyl-4-methoxy-5-fluoroacetylaminophenol
https://huagongshe.com/reaction/1030001
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzene | HCID 241 | — |
| Reactant | Methyl fluoroacetate | HCID 9959 | — |
| Reactant | Phenol, 5-amino-4-methoxy-2-methyl- | HCID 10197787 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Methyl-4-methoxy-5-fluoroacetylaminophenol | HCID 19821151 | 13.9% |
Reaction Steps
Into 15 ml of benzene were added 2.10 g (13.7 mmol) of 2-methyl-4-methoxy-5-aminophenol, 1.28 g (13.9 mmol, 1.0 eq.) of methyl fluoroacetate and 1.64 g (30.4 mmol) of sodium methoxide and the mixture was heated under reflux for 6.5 hours. After allowing to cool, the mixture was poured into 300 ml of water, and neutralized with acetic acid and extracted with 200 ml of ethyl acetate. The organic layer was washed with a saturated aqueous solution of common salt and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain dark-brown crystals. The crystals were purified by silica gel column chromatography (Silica Gel 60, trade name, manufactured by Merck Co., 70-230 mesh, 200 g, eluent: ethyl acetate) and pale brown solid matters were obtained from the 600-900 ml fraction. The solid matters were recrystallized from the solvent mixture of hexane/ethyl acetate (2:1 by volume) to give 230 mg (1.9 mmol) of 2-methyl-4-methoxy-5-fluoroacetylaminophenol. The yield was 8%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05104414 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-f29c70e8284d432d93209922d4ffd944 |
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| Source note | uspto-grants-1992_04 |
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