HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → 2-Benzylthio-2-thiazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178527880 | HCID 178527880 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Benzylthio-2-thiazoline | HCID 275677 | 258.8% |
Reaction Steps
To a dry, nitrogen (N2)-purged 500 milliliter (mL) round bottom flask was added 1.15 grams (g) (4.8 mmol) sodium hydride. To this was added 150 mL dry tetrahydrofuran and 5.70 g (4.8 mmol) 2-mercaptothiazoline in 24 mL tetrahydrofuran. After approximately 15 minutes of stirring at room temperature, 5.5 mL (4.8 mmol) benzyl chloride was added and stirred for an additional 5 minutes. Tetrahydrofuran was removed by rotary evaporation and product was dissolved in hexane. After filtration, the product was recrystallized from hexane to yield 2.6 g of white crystals (26% yield). 1H NMR (CDCl3): 3.434 ppm, t, 2H; 4.259 ppm, t, 2H; 4.413 ppm, s, 2H; 7.317 ppm, m, 5H.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723440B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-e26ac105580344a7b6a2511150fd1477 |
| Source note | uspto-grants-2010_05 |