HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Dimethylamino)-1-phenyl-1-propanone → alpha-(1-Methyl-2-pyrrolidinyl)acetophenone 2,4,6-triisopropylbenzenesulphonylhydrazone hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Dimethylamino)-1-phenyl-1-propanone | HCID 77042 | — |
| Reactant | 2,4,6-Triisopropylbenzenesulphonohydrazide | HCID 359333 | — |
| Reactant | alpha-(1-Methyl-2-pyrrolidinyl)acetophenone hydrochloride | HCID 20133696 | — |
| 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 of a white solid melting at 210° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04686309 |
| Source dataset | uspto-grants-1987_08 |
| ORD ID | ord-e86a3e9ff2604fdf978a729dc5841fcf |
| Source note | uspto-grants-1987_08 |