HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 4-Ethyl-2-thiophenemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-Ethylthiophene-2-carbaldehyde | HCID 15209622 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Ethyl-2-thiophenemethanol | HCID 23261287 | 100% |
Reaction Steps
4-Ethyl-2-thiophenecarbaldehyde (1 g, 7.13 mmol) dissolved in methanol (7 ml) was added with sodium borohydride (135 mg, 3.57 mmol) under ice cooling, stirred for 10 minutes and then further added with sodium borohydride (150 mg, 3.96 mmol) at 0° C. After the reaction solution was stirred under ice cooling for 30 minutes, the reaction was stopped with saturated aqueous ammonium chloride and the reaction solution was extracted with chloroform. The organic layer collected was dried over magnesium sulfate and concentrated under reduced pressure to obtain 1 g (100%) of the title compound without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07056917B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-ccaa916835af4b6f91c4d27618e9e2b7 |
| Source note | uspto-grants-2006_06 |