HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 59277703, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 59277705 | HCID 59277705 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59277703 | HCID 59277703 | 100% |
Reaction Steps
NaBH4 (45 mg, 1.2 mmol) is added to a solution of 1,3,3-Trimethyl-2,2-dioxo-2,3-dihydro-1H-benzo[c][1,2]thiazin-4-one (190 mg, 0.8 mmol) in 15 mL of EtOH at 0° C. The resulting mixture is stirred at this temperature for overnight. The reaction is quenched by HCl (1M), and extracted with ethyl acetate (15 mL×3). The combined extracts are dried over anhydrous Na2SO4. After filtration and concentration, the residue is purified by flash column and yields the title compound as oil (193 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143278B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-20043f9432974a28b0460af2f9fb8491 |
| Source note | uspto-grants-2012_03 |