HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 68973728, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 68971896 | HCID 68971896 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68973728 | HCID 68973728 | — |
Reaction Steps
At ambient temperature, to 0.83 g (1.72 mmol) of the compound obtained in Step C of Example 84, dissolved in 32 mL of acetonitrile, there are added, all at once, 1.4 mL (17.2 mmol) of 37% aqueous formaldehyde solution and then 0.22 g (3.44 mmol) of sodium cyanoborohydride. After stirring for 45 minutes at ambient temperature, concentration is carried out and the residue is taken up in 30 mL of water; the aqueous phase is extracted twice with 30 mL of dichloromethane; the organic phases are combined, washed with 30 mL of water and dried over magnesium sulphate. After concentration, the residue is chromatographed over silica (eluant: dichloromethane/ethanol/ammonia 95/5/0.5) to yield the desired compound in the form of the base.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08076325B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-cecdc60b877844b388882fc4b8e06adc |
| Source note | uspto-grants-2011_12 |