HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Thioglycolate → 118286-24-1
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Thioglycolate | HCID 16907 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Bromodiphenylmethane | HCID 236603 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 118286-24-1 | HCID 11231102 | 15% |
Reaction Steps
To a solution of methyl thioglycolate (5.95 g, 56 mmol) in 225 mL of tetrahydrofuran is added sodium hydride (2.5 g of 60% NaH in oil, 62.5 mmol). The mixture is stirred at room temperature for 10 minutes. Benzhydryl bromide (Aldrich of Milwaukee, Wis.; hereinafter "Aldrich") (15.3 g, 62 mmol) is added and the reaction mixture is stirred at room temperature for 3 days and then concentrated in vacuo. The residue is taken up in ethyl acetate and washed with saturated aqueous sodium bicarbonate, 10% aqueous citric acid, and brine and then dried over magnesium sulfate. Chromatography on silica gel, eluting with 4% ethyl acetate in hexane provides methyl [[(diphenyl)methyl]thio]acetate as a colorless oil in 15% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05571825 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-29e91dd8b92946d38904017ecd4e16bf |
| Source note | uspto-grants-1996_11 |