HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 67828174, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 57129736 | HCID 57129736 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 67828174 | HCID 67828174 | — |
Reaction Steps
31.2 g of 1-(4-Carbo-tert.-butoxyphenyl)-2-(4'-carbethoxybiphenyl-4-yl)-ethene in 150 ml of absolute toluene are boiled under reflux for 3 hours with 1 g of p-toluene sulphonic acid. The reaction mixture is then evaporated to dryness, 8.68 g of NaOH in 100 ml of H2O and 100 ml of ethanol are added, and the mixture is boiled for 4 hours. It is then filtered hot after the addition of active charcoal, diluted with 200 ml of H2O and extracted twice with CH2Cl2, and the product is precipitated from the aqueous phase with conc. HCl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05068300 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-3391d2e4954f4fea86dc6fcaf00f4879 |
| Source note | uspto-grants-1991_11 |