HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493048Generated: October 30, 2026
Water → 5-Acetylamino-2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran
https://huagongshe.com/reaction/1493048
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Amino-2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran | HCID 10035862 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Acetylamino-2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran | HCID 10776887 | 76.4% |
Reaction Steps
Acetyl chloride (460 mg, 5.84 mmol) was added dropwise with ice cooling to a solution of 5-amino-2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran (100g, 4.87 mmol) and triethylamine (640 mg, 6.33 mmol) in tetrahydrofuran (20 ml). After the addition was completed, the mixture was stirred for 4 hours. Water was added to the reaction mixture and the mixture was extracted with chloroform. The extract was washed with saturated sodium bicarbonate solution and saturated saline, dried and concentrated. The residue was purified by column chromatography on silica gel (chloroform-methanol, 97:3) to obtain the desired compound (920 mg, yield: 76.4%). A part of it was recrystallized from dichloromethane-isopropyl ether, m.p. 190° C. (dichloromethane-isopropyl ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05376681 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-f7b30947f53d4eac9153d1f7eb484f95 |
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| Source note | uspto-grants-1994_12 |
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