HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 1-(Hydroxymethyl)-cyclohexanecarboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Cyclohexanecarboxaldehyde | HCID 16275 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 1-(Hydroxymethyl)-cyclohexanecarboxaldehyde | HCID 13106397 | 59.7% |
Reaction Steps
To a cold (0° C. mixture of 100 g (0.891 mole) of cyclohexanecarboxaldehyde, 76.5 g of 37% of formaldehyde in 225 ml of mnethanol was added dropwise 90 ml of 1 N Sodium hydroxide in 1 h. The reaction mixture was stirred at room temperature over 48 then was evaporated to remove methanol. The reaction mixture was diluted with water and extracted with methylene chloride. The organic layer was washed with water, brine, and dried over sodium sulfate and concentrated under vacuum to give 75 g (59.7%) of thick oil. Proton NMR and mass spectra were consistent with the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06943189B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-1ea640c14e8b4278934aa3a1f18414c8 |
| Source note | uspto-grants-2005_09 |