HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-Chlorophenyl)-2-butyn-1-ol → (Z)-1-(4-chlorophenyl)-2-buten-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-Chlorophenyl)-2-butyn-1-ol | HCID 20188339 | — |
| Catalyst | Lindlars catalyst | HCID 131709914 | — |
| Product | (Z)-1-(4-chlorophenyl)-2-buten-1-ol | HCID 67901371 | — |
Reaction Steps
Under nitrogen, hydrogenate a mixture of 10 g (0.055 mole) of 1-(4-chlorophenyl)-2-butyn-1-ol and 0.6 g Lindlar catalyst. Following the reaction via NMR the reaction is complete in about two days. The hydrogenation is stopped and the reaction stirred under N2 at room temperature overnight. Filter off the catalysts, wash with methylene chloride combine the filtrate and evaporate to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04581370 |
| Source dataset | uspto-grants-1986_04 |
| ORD ID | ord-413af3631eaf47fdb58ab7913b111ccb |
| Source note | uspto-grants-1986_04 |