HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 2-Hydroxymethyl-2-phenylheptanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Phenylheptanenitrile | HCID 12652020 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Hydroxymethyl-2-phenylheptanenitrile | HCID 66987852 | 71% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
5.14 g (27.4 mmol) of 2-phenylheptanenitrile are added to a suspension of 1.34 g of 60% NaH in 50 ml of DMF cooled to 0° C. After stirring for 30 minutes, 7.6 g (220 mmol) of paraformaldehyde are added portionwise. The reaction medium is left to stir at ambient temperature for 6 hours and then hydrolysed with ice and extracted with diethyl ether. The organic phase is washed with a saturated aqueous solution of sodium hydrogen carbonate, dried over sodium sulphate, filtered and evaporated under pressure. The crude product obtained is purified by silica gel chromatography (eluent 8/2 heptane/ethyl acetate). 4.24 g in the form of a pale yellow oil are obtained with a yield of 71%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08871187B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-16b9849e45e9416fa2bfd3498008499e |
| Source note | uspto-grants-2014_10 |