HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Chloromethyl-2-methoxy-1-pent-2-ynyloxy-benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (3-Methoxy-4-pent-2-ynyloxy-phenyl)-methanol | HCID 18442092 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-Chloromethyl-2-methoxy-1-pent-2-ynyloxy-benzene | HCID 18442093 | — |
Reaction Steps
A solution of (3-methoxy-4-pent-2-ynyloxy-phenyl)-methanol (27 g, 0.12 mol) in 450 ml of dioxan is added dropwise to 240 ml of concentrated hydrochloric acid. The reaction mixture is stirred for 1.5 hours at room temperature. Subsequently it is poured on water and extracted with ethyl acetate. The combined organic layer is washed with brine, dried over magnesium sulfate and evaporated in vacuo to obtain 4-chloromethyl-2-methoxy-1-pent-2-ynyloxy-benzene as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07189873B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-7a630b6eee2b467e860d1d0089b0a612 |
| Source note | uspto-grants-2007_03 |