HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651812Generated: November 1, 2026
4-Methylbenzaldehyde → HCID 23050515, compound
https://huagongshe.com/reaction/1651812
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylbenzaldehyde | HCID 7725 | — |
| Reactant | Methyl propiolate | HCID 13536 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23050515 | HCID 23050515 | — |
Reaction Steps
A solution of 8.4 ml (0.1 mol) of methyl propiolate in 100 ml of tetrahydrofuran was treated at -78° under argon with 68.8 ml of n-butyllithium (1.6M in hexane). The mixture was stirred at -78° for 10 minutes and then a solution of 11.8 ml (0.1 mol) of 4-methylbenzaldehyde in 100 ml of tetrahydrofuran was added within 40 minutes. The reaction mixture was stirred at -78° for a further 20 minutes, then brought to room temperature and treated with 100 ml of saturated ammonium chloride solution The aqueous phase was extracted twice with ether. The combined organic phases were washed in succession with saturated sodium chloride solution and with water, dried over sodium sulphate and concentrated. The residue was purified by flash chromatography on 1000 g of silica gel (elution agent methylene chloride/ethyl acetate 9:1). There was obtained methyl 4-hydroxy-4-(4-methylphenyl)-2-butynoate as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04929741 |
|---|
| Source dataset | uspto-grants-1990_05 |
|---|
| ORD ID | ord-72388fbc065f43bc942214171b9b6005 |
|---|
| Source note | uspto-grants-1990_05 |
|---|