HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 54526089, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Tetrahydrofurfuryl alcohol | HCID 7360 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 54049431 | HCID 54049431 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Product | HCID 54526089 | HCID 54526089 | — |
Reaction Steps
A solution of [4-(3-amino-benzoylamino)-phenyl]-carbamic acid t-butyl ester (505 mg), sodium cyanoborohydride (250 mg), acetic acid (3 drops) and 40% aqueous formaldehyde (4 mL) in 1:2 tetrahydrofuran-methanol (15 mL) is stirred for 15 minutes, and then poured into saturated aqueous sodium bicarbonate and extracted into ethyl acetate. The ethyl acetate solution is dried over anhydrous potassium carbonate and concentrated under reduced pressure to give a solid which is recrystallized from acetonitrile to provide a pale pink crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06403617B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-0a315fb479a441c9802e22916fe717e9 |
| Source note | uspto-grants-2002_06 |