HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinuclidine → Benzyl-(4-isothiocyanatobenzyl)dimethyl-ammonium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinuclidine | HCID 7527 | — |
| Reactant | N,N-Dimethylbenzylamine | HCID 7681 | — |
| Reactant | 3-Bromopropyl isothiocyanate | HCID 137714 | — |
| Reactant | 1-(Bromomethyl)-4-isothiocyanatobenzene | HCID 10242862 | — |
| Product | Benzyl-(4-isothiocyanatobenzyl)dimethyl-ammonium bromide | HCID 23074198 | — |
Reaction Steps
The procedure in the step a in Example 9 was followed except that instead of 3-bromopropyl isothiocyanate, 4-(bromomethyl)phenyl isothiocyanate (is-14 mentioned earlier) was used and instead of quinuclidine, N,N-dimethylbenzylamine (ta-32 mentioned earlier) was used to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07803792B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-8fd86c2cb58e469fb0c5a3726afcb34e |
| Source note | uspto-grants-2010_09 |