HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4'-tert-Butyl-2,6-dimethyl-biphenyl-4-thiol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | dimethyl-thiocarbamic acid S-(4'-tert-butyl-2,6-dimethyl-biphenyl-4-yl) ester | HCID 86625172 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4'-tert-Butyl-2,6-dimethyl-biphenyl-4-thiol | HCID 59356048 | 83.7% |
Reaction Steps
To a solution of dimethyl-thiocarbamic acid S-(4′-tert-butyl-2,6-dimethyl-biphenyl-4-yl) ester (8.8 g, 25.8 mmol) in methanol (65 mL) is added sodium methoxide (1.39 g, 25.8 mmol). The reaction mixture is heated to reflux overnight. After cooling to room temperature, the reaction mixture is neutralized with 5N HCl, concentrated to ⅓ volume, treated with brine, and extracted into dichloromethane. The aqueous layer is back-extracted with dichloromethane, and the combined organic layers are dried and concentrated. The resulting residue is applied to silica gel and eluted using hexanes with an ethyl acetate gradient from 0% to 50% to give the title compound (5.84 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07807702B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-80d5f6cf6e7c491fb9c98e40707eaf38 |
| Source note | uspto-grants-2010_10 |