HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 54161335, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Propanesulfonyl chloride | HCID 82408 | — |
| Reactant | HCID 59115184 | HCID 59115184 | — |
| Product | HCID 54161335 | HCID 54161335 | 83% |
Reaction Steps
Analogously to the preparation of Example 3.4, 9.6 g (0.5 mol) of α-hydroxyimino-4-methylthiobenzyl cyanide are reacted, in the presence of 7.6 g (0.075 mol) of triethylamine, with 7.85 g (0.055 mol) of 2-propanesulfonyl chloride. After working-up, the crude product is recrystallised from acetic acid acetate/hexane. 11.1 g (83%) of α-(2-propylsulfonyloxyimino)-4-methylthiobenzyl cyanide are obtained in the form of beige crystals having a melting point of 83-87° C. The 1H-NMR spectrum of the compound shows that it is a pure stereoisomer. The UV spectrum (acetonitrile) of the substance shows a broad absorption band with a maximum at 350 nm (ε=14660) that extends to 435 nm. Elemental analysis: C12H14N2O3S2 (266.32)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06017675 |
| Source dataset | uspto-grants-2000_01 |
| ORD ID | ord-9d7b7e4b5902445aae179b7418e3a481 |
| Source note | uspto-grants-2000_01 |