HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetyl chloride → 3-(Phenylacetyl)-2-nitromethylene-tetrahydro-2H-1,3-thiazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-nitromethylenetetrahydro-2H-1,3-thiazine | HCID 42853 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(Phenylacetyl)-2-nitromethylene-tetrahydro-2H-1,3-thiazine | HCID 53896588 | — |
Reaction Steps
To a solution of phenylacetyl chloride (4.8 g) in dry dichloromethane (30 ml) at -20° C. was added triethylamine (5.2 ml) over a period of 20 minutes, followed by 2-(nitromethylene)-tetrahydro-2H-1,3-thiazine (3.2 g) in dry dichloromethane (30 ml) over a period of 20 minutes. The reaction mixture was allowed to warm to ambient temperature with stirring over a period of 30 minutes and was then worked up in a similar manner to that described in Example 1 to yield the required product as a white crystalline solid m.p. 121°-122° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04529726 |
| Source dataset | uspto-grants-1985_07 |
| ORD ID | ord-a49b3e79590b499e923373739244dbc7 |
| Source note | uspto-grants-1985_07 |