HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2-chloro-4-(methylthio)benzoate → HCID 54209533, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2-chloro-4-(methylthio)benzoate | HCID 13961932 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54209533 | HCID 54209533 | 103.3% |
Reaction Steps
To a suspension of lithium aluminum hydride (139 mg) in tetrahydrofuran (8 ml) was added dropwise methyl 2-chloro-4-(methylthio)benzoate (806 mg) under ice-cooling, and the mixture was stirred for 1 hr. The reaction mixture was diluted with diethyl ether and 1N hydrochloric acid (10 ml) was added dropwise. The resulting product was extracted 3 times with diethyl ether. The organic layers were combined and washed successively with saturated aqueous sodium hydrogencarbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated to give 2-chloro-4-(methylthio)benzyl alcohol (725 mg) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07060721B1 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-19b2a89483364920af1f0e09f2970600 |
| Source note | uspto-grants-2006_06 |