HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 67234479, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Bromocresol Green | HCID 6451 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 67235025 | HCID 67235025 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67234479 | HCID 67234479 | — |
Reaction Steps
Aqueous formaldehyde 37% (12.6 mmol) is added to a suspension of the product of Example 8 (2.52 mmol) in 10 ml of acetonitrile. The suspension is stirred for 1 hour at ambient temperature. A spatula tip of bromocresol green and sodium cyanoborohydride (7.56 mmol) are added in succession. The reaction mixture is brought to acid pH by adding 4N HCl solution in dioxane. The reaction mixture is stirred overnight at ambient temperature and is then neutralised by addition of 10% NaHCO3 solution. After diluting the reaction mixture with water, a precipitate forms, which is filtered off. Purification of the title product is carried out by chromatography on silica, eluting with a mixture of dichloromethane/ethyl acetate 96/4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08236790B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-a2f174fb53f544d0930a867cbe308584 |
| Source note | uspto-grants-2012_08 |