HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 1-(2-Thienyl)benzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Thiophene, 2-(phenylmethyl)- | HCID 139391 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 1-(2-Thienyl)benzyl alcohol | HCID 69947985 | 92% |
Reaction Steps
Sodium borohydride (0.37 g, 10 mmol) was added to 2-benzylthiophene (1.88 g, 10 mmol) dissolved in methanol/THF mixture (1:10 ratio, 11 ml). This was stirred at room temperature for 10 h. The reaction mixture was decomposed by addition of saturated ammonium chloride solution (50 ml) and was extracted with ethyl acetate (2×50 ml). The combined organic layer was dried over anhydrous MgSO4. Removal of the solvent gave 1-(2-thienyl)benzyl alcohol as a solid (1.75 g, 92% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05571821 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-20471e16f5c446b88a39a30041c66474 |
| Source note | uspto-grants-1996_11 |