HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4,6-Triisopropylbenzenesulphonohydrazide → alpha-(1-Methyl-2-pyrrolidinyl)acetophenone 2,4,6-triisopropylbenzenesulphonylhydrazone hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4,6-Triisopropylbenzenesulphonohydrazide | HCID 359333 | — |
| Reactant | alpha-(1-Methyl-2-pyrrolidinyl)acetophenone hydrochloride | HCID 20133696 | — |
| Reactant | beta-Dimethylaminopropiophenone 2,4,6-triisopropylbenzenesulphonylhydrazone | HCID 86741729 | — |
| Reactant | alpha-(1-Methyl-2-pyrrolidinyl)acetophenone 2,4,6-triisopropylbenzenesulphonylhydrazone | HCID 86741735 | — |
| Product | alpha-(1-Methyl-2-pyrrolidinyl)acetophenone 2,4,6-triisopropylbenzenesulphonylhydrazone hydrochloride | HCID 86741734 | — |
Reaction Steps
α-(1-Methyl-2-pyrrolidinyl)acetophenone 2,4,6-triisopropylbenzenesulphonylhydrazone can be prepared by a method similar to that described in Example 22 for the preparation of β-dimethylaminopropiophenone 2,4,6-triisopropylbenzenesulphonylhydrazone, but starting from 2,4,6-triisopropylbenzenesulphonylhydrazine (30.6 g) and α-(1-methyl-2-pyrrolidinyl)acetophenone hydrochloride (28.3 g). In this way, α-(1-methyl-2-pyrrolidinyl)acetophenone 2,4,6-triisopropylbenzenesulphonylhydrazone hydrochloride (31.1 g) is obtained in the form a white solid melting at 210° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04755599 |
| Source dataset | uspto-grants-1988_07 |
| ORD ID | ord-04bf7de5a05d404b8d0f79c21b09b904 |
| Source note | uspto-grants-1988_07 |