HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 9857138, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22473925 | HCID 22473925 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 9857138 | HCID 9857138 | 86.9% |
Reaction Steps
Sodium borohydride (0.05 g) was added in portions over 2 minutes to a stirred suspension of 3-(benzo[b]thiophen-4-yl)-5,6-dihydroimidazo[2,1-b]thiazole-2-carboxaldehyde (0.36 g) in methanol (10 ml), then the mixture was stirred at ambient temperature for 1.5 hours. The solvent was removed in vacuo then water (20 ml) and ethyl acetate (30 ml) were added and the mixture was stirred at ambient temperature for 2 hours. The aqueous phase was separated and washed with ethyl acetate (30 ml), then the combined ethyl acetate solutions were dried (MgSO4) and the solvent was removed in vacuo at 60° C. to give [3-(benzo[b]thiophen-4-yl)-5,6-dihydroimidazo[2,1-b]thiazol-2-yl]methanol (0.315 g) as a cream solid, m.p. 145-149° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06900216B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-958abc5ee033498e93a9b4f02c99796c |
| Source note | uspto-grants-2005_05 |