HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-Chloro-2-(1-ethoxyiminobutyl)-5-(tetrahydrothiopyran-3-yl)cyclohex-2-en-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Cycloxydim | HCID 135499147 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Chloro-2-(1-ethoxyiminobutyl)-5-(tetrahydrothiopyran-3-yl)cyclohex-2-en-1-one | HCID 54430237 | — |
Reaction Steps
10.0 g (31 mmol) of 2-(1-ethoxyiminobutyl-3-hydroxy-5-(tetrahydrothiopyran-3-yl)cyclohex-2-en-1-one were dissolved in 50 ml of tetrahydrofuran, and 4.7 ml of triethylamine were added, followed by 2.3 ml of thionyl chloride. After 3 hours the resulting precipitate was filtered off with suction, and washed with tetrahydrofuran, and the product-containing filtrate was concentrated. 3-Chloro-2-(1-ethoxyiminobutyl)-5-(tetrahydrothiopyran-3-yl)cyclohex-2-en-1-one was obtained as an oil (compound no. 90).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04761486 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-26076139a64545109d2ebff3b9ac8de0 |
| Source note | uspto-grants-1988_08 |