HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38488Generated: October 28, 2026
Acetic Anhydride → HCID 178497281, compound
https://huagongshe.com/reaction/38488
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Isobutyl nitrate | HCID 10974 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Methyl 3-amino-4-ethylbenzoate | HCID 13399999 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178497281 | HCID 178497281 | — |
Reaction Steps
Ac2O (0.579 ml, 6.14 mmol) was added to a stirred mixture of KOAc (361 mg, 3.68 mmol) and methyl 3-amino-4-ethylbenzoate (550mg, 3.07 mmol) in CHCl3 (5 ml) and the mixture was stirred at 90° C. for 2 h. KOAc (361 mg, 3.68 mmol), 18-crown-6 ether (81 mg, 0.307 mmol) and isobutylnitrate (719 mg, 6.14 mmol) were added thereto at room temperature and the mixture was further stirred at 90° C. for 2 h. The reaction mixtuer was diluted with chloroform and H2O, the organic layer was washed with water, brine, and dried over MgSO4. After filteration and evaporation, the residue was diluted with THF (5.00 ml) and MeOH (5.00 ml), and K2CO3 (848 mg, 6.14 mmol) was added thereto at room temperature. After the mixture was stirred for 2 h. at room temperature, CHCl3 and H2O was added thereto. The organic layer was washed with H2O, brine, and dried over MgSO4. After filteration and evaporation, the reside was puritied by silicagel column chromatography (hexane/EtOAc) to give intended compound as a pale brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524730B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-4fec3f76bc8444e8909bfaad57ee46ee |
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| Source note | uspto-grants-2013_09 |
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