HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl bromide → 4-[(2-Propynyloxy)methyl]benzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | 1,4-Benzenedimethanol | HCID 11506 | — |
| Product | 4-[(2-Propynyloxy)methyl]benzyl alcohol | HCID 54520131 | — |
Reaction Steps
In an analogous manner to that described in Example 1, from 4-(hydroxymethyl)benzyl alcohol and propargyl bromide there is obtained 4-[(2-propynyloxy)methyl]benzyl alcohol. This alcohol is reacted in an analogous manner to that described in Example 2 with cyclopropane carboxylic acid chloride to give cyclopropane carboxylic acid p-[(2-propynyloxy)methyl]benzyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04162328 |
| Source dataset | uspto-grants-1979_07 |
| ORD ID | ord-4012781ca93f49b08510409f1f36f07c |
| Source note | uspto-grants-1979_07 |