HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromomethylnaphthalene → 2-Naphthylmethyl ethanimidothioate hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromomethylnaphthalene | HCID 70320 | — |
| Reactant | Thioacetamide | HCID 2723949 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Naphthylmethyl ethanimidothioate hydrobromide | HCID 22138705 | 78.6% |
Reaction Steps
Thioacetamide (326.0 mg, 4.339 mmol) and 2-bromomethyl-naphthalene (959.0 mg, 4.337 mmol) were placed in a 50 mL round-bottom flask. 20 mL of CHCl3 were added and the mixture was refluxed for 3 h at which time a white precipitate formed. The mixture was cooled and the precipitate collected. The precipitate was washed with 20 mL of CH2Cl2 and placed under vacuum for drying to give 1.01 g of thioacetimidic acid naphthalen-2-ylmethyl ester hydrobromide salt as a fine white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07405225B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-aa40cb0bdfda4a8f9a128849bacec49c |
| Source note | uspto-grants-2008_07 |