HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3',4'-dihydro-4'-hydroxy-7'-fluorospiro[imidazolidine-4,1'(2'H)-naphthalene]2,5-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 13563112 | HCID 13563112 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3',4'-dihydro-4'-hydroxy-7'-fluorospiro[imidazolidine-4,1'(2'H)-naphthalene]2,5-dione | HCID 13563097 | 47% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 15.5 g. (0.0625 mole) of 3',4'-dihydro-7'-fluorospiro [imidazolidine-4,1'(2'H)-naphthalene]2,4',5-trione in 300 ml. of methanol cooled to 0° C. was added 4.8 g. (0.012 mole) of sodium borohydride over a period of 20 minutes. After stirring for one hour at 0° C. 100 ml. of 10% hydrochloric acid was added and the methanol removed under vacuum. The solid suspension was filtered and the solids dried, 7.3 g. (47% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04575507 |
| Source dataset | uspto-grants-1986_03 |
| ORD ID | ord-bab1ecc67f0a4cb8b7d86cfdc4374ae8 |
| Source note | uspto-grants-1986_03 |