HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245776Generated: October 25, 2026
Toluene → 4-(4-Dimethylaminophenylsulfanyl)-2-methylpent-2-en-1-ol
https://huagongshe.com/reaction/2245776
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | 4-(4-Dimethylaminophenylsulfanyl)-2-methylpent-2-enoic acid methyl ester | HCID 68545878 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(4-Dimethylaminophenylsulfanyl)-2-methylpent-2-en-1-ol | HCID 68543121 | 88% |
Reaction Steps
To a solution of 4-(4-dimethylaminophenylsulfanyl)-2-methylpent-2-enoic acid methyl ester (0.279 g, 1.0 mmol) in dry THF (4 mL) at 0° C. was added dropwise a solution of di-isobutylaluminium hydride in toluene (1M, 3.0 mL, 3.0 mmol), under an atmosphere of argon. After stirring at 0° C. for one hour (TLC monitoring), the mixture was quenched by addition of methanol (0.5 mL: CAUTION), then water (0.3 mL), 5% aqueous sodium hydroxide solution (0.3 mL) and lastly 30% aqueous sodium potassium tartrate (4 mL). The mixture was stirred for 2 hours at 20° C., then extracted with diethyl ether (3×10 mL). The combined organic layers were dried over anhydrous MgSO4, filtered and evaporated to give the title compound (0.22 g, 88%) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07683185B2 |
|---|
| Source dataset | uspto-grants-2010_03 |
|---|
| ORD ID | ord-ec9bfa5c612143cd99f27e6e868d2997 |
|---|
| Source note | uspto-grants-2010_03 |
|---|