HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 2,3-Dihydro-3,3-dimethyl-2-methylcarbonyloxybenzofuran-5-yl dimethylaminosulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 21445718 | HCID 21445718 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,3-Dihydro-3,3-dimethyl-2-methylcarbonyloxybenzofuran-5-yl dimethylaminosulfonate | HCID 21445723 | — |
Reaction Steps
At -8°C to -12°C and while stirring, 10.3 parts by weight of acetyl chloride was added to a solution of 28.7 parts by weight of 2,3-dihydro-3,3-dimethyl-2-hydroxybenzofuran-5-yl dimethylaminosulfonate and 14.1 parts by weight of triethylamine in 110 parts by weight of ether. The mixture was worked up as in Example 1, the compound 2,3-dihydro-3,3-dimethyl-2-methylcarbonyloxybenzofuran-5-yl dimethylaminosulfonate being obtained in the form of crystals; melting point: 67° to 68°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04014904 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-aa17a852b0c740daa162815de6210135 |
| Source note | uspto-grants-1977_03 |