HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-Allyloxy-4-chloromethyl-benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (4-(Prop-2-en-1-yloxy)phenyl)methanol | HCID 11744970 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Allyloxy-4-chloromethyl-benzene | HCID 12347936 | — |
Reaction Steps
7.67 g (67.0 mmol) methanesulfonyl chloride were given at 0° C. to a solution of 10.0 g (60.9 mmol) (4-allyloxy-phenyl)-methanol and 9.34 ml (67.0 mmol) triethylamine in 35 ml dichloromethane and stirred at r.t. overnight. The mixture was poured in ice water, extracted with dichloromethane and the organic phase dried over Na2SO4. After removal of solvents the residue was purified by chromatography on silica gel (ethyl acetate/n-heptane 1:5) to yield 3.12 g (28%) pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07235574B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-a4bb0bfb1f524dbeb1f90661deb84a55 |
| Source note | uspto-grants-2007_06 |