HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glyoxylic Acid → HCID 18620256, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glyoxylic Acid | HCID 760 | — |
| Reactant | 2-(tert-Butyl)-4-chlorophenol | HCID 518765 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 18620256 | HCID 18620256 | 31.5% |
Reaction Steps
2.8 g of 2-tert-butyl-4-chlorophenol [J. Amer. Chem. Soc. 78, 4604 (1956)] are refluxed for 3¼ h with 2.45 g of 50% aqueous glyoxylic acid and 50 mg of p-toluenesulfonic acid in 20 ml of 1,2-dichloroethane. Thereafter a further 2.45 g of 50% aqueous glyoxylic acid are added to continue refluxing for 18 h. The reaction mixture is then washed with water, dried over MgSO4 and evaporated in a rotary evaporator. Crystallization of the residue from hexane leaves 1.15 g of 7-tert-butyl-5-chloro-3-hydroxy-3H-benzofuran-2-one (melting point: 150-154° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06323267B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-0e058f2e105b4405b7e6b191381a9946 |
| Source note | uspto-grants-2001_11 |