HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Sulfate → HCID 12495247, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Sulfate | HCID 6163 | — |
| Reactant | HCID 54358704 | HCID 54358704 | — |
| Product | HCID 12495247 | HCID 12495247 | — |
Reaction Steps
Compound B) is transformed into the corresponding p-toluene sulfonamido derivative (M.p. 230°-33° C) by reaction with p-toluenesulfonychloride. This compound is subsequently reacted in strong alkaline solution with diethylsulfate, thus obtaining 4-benzoyl-3-(N-ethyl-p-toluenesulfonamido)-5-methyl-2-phenyl-pyrrole (M.p. 152°-53° C), which is in turn converted into the title compound (B.p. 220° C/0.015 mmHg) by acid hydrolysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03993650 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-edff8aefdb01463c82fcfe7f6bd11596 |
| Source note | uspto-grants-1976_11 |