HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-Chloro-4-methylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Chloro-4-methylbenzyl alcohol | HCID 123486 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 3-Chloro-4-methylbenzaldehyde | HCID 12423085 | 70.9% |
Reaction Steps
To a solution of 3-chloro-4-methylbenzyl alcohol (2.00 g) and triethylamine (8.9 ml) in a dimethyl sulfoxide (10 ml) was added sulfur trioxide-pyridine complex (4.47 g) under ice-cooling, and the mixture was stirred at room temperature for 3 hr. The reaction mixture was poured into ice water, and extracted with ether. The organic layer was washed with 1N hydrochloric acid, saturated brine and a saturated aqueous sodium hydrogencarbonate solution, dried over magnesium sulfate, and concentrated to dryness under reduced pressure to give the objective compound (1.40 g) as a pale-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06911469B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-b4620fcd7c954d86942a6dccf0e9c7d1 |
| Source note | uspto-grants-2005_06 |