HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-1-chloroethane → 3-(2-Chloroethyl)-7,7,9,9-tetramethyl-1,3,8-triazaspiro[4.5]decane-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-1-chloroethane | HCID 11654 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 7,7,9,9-Tetramethyl-1,3,8-triazaspiro[4.5]decane-2,4-dione | HCID 1268066 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(2-Chloroethyl)-7,7,9,9-tetramethyl-1,3,8-triazaspiro[4.5]decane-2,4-dione | HCID 59355191 | — |
Reaction Steps
A mixture of 7,7,9,9-tetramethyl-1,3,8-triazaspiro[4.5]decane-2,4-dione (5, 22.2 mmol) and KOH (1.24 g, 22.2 mmol) in EtOH was refluxed for 10 min and bromochloroethane (6.35 g, 44.4 mmol) was added and refluxing continued for additional 6 h. Filtered and concentrated to get the crude chloroethylated product which was used as such for the next step (5.5 g). LCMS—[M+H] m/z 228.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08722715B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-fd171ac22d1b464b8671e2f36b6dd81c |
| Source note | uspto-grants-2014_05 |