HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 1-[2-(4-Allyloxy-2-methyl-benzyloxy)-ethyl]-1H-[1,2,3]triazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(1H-1,2,3-triazol-1-yl)ethan-1-ol | HCID 9989237 | — |
| Reactant | 1-Allyloxy-4-chloromethyl-2-methyl-benzene | HCID 22242077 | — |
| Product | 1-[2-(4-Allyloxy-2-methyl-benzyloxy)-ethyl]-1H-[1,2,3]triazole | HCID 69293375 | 86% |
Reaction Steps
1.122 g (46.7 mmol) 95% Sodium hydride were given at −50° C. to a solution of 5.630 g (31.2 mmol) 1-allyloxy-4-chloromethyl-2-methyl-benzene and 3.525 g (31.2 mmol) 2-(1H-[1,2,3]-triazol-1-yl)-ethanol in DMF. The mixture was allowed to warm slowly to r. t., stirred for 5 hours. The mixture was concentrated in vacuo and the residue was partitioned between ethyl acetate and water. The organic layer was dried over Na2SO4 and the solvent was distilled off under reduced pressure to yield 7.30 g (86%) 1-[2-(4-Allyloxy-2-methyl-benzyloxy)-ethyl]-1H-[1,2,3]triazole as yellow oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07432291B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-125b9993e35d48ba8863cd6da0f22eda |
| Source note | uspto-grants-2008_10 |