HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 178466054, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 178466053 | HCID 178466053 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178466054 | HCID 178466054 | — |
Reaction Steps
To a suspension of 0.128 part of 6-acetyl-3-(1H-tetrazol-5-yl)chromone in 5 parts by volume of methanol is added under stirring 0.020 part of sodium borohydride. The resulting mixture is stirred at room temperature for 2 minutes and then refluxed for 2 minutes. The solvent is distilled off and to the residue is added 10 parts by volume of 1N-hydrochloric acid. The resulting precipitates are recovered by filtration and recrystallized twice from ethanol to obtain 0.013 part of 6-(1-hydroxyethyl)-3-(1H-tetrazol-5-yl)chromone as colorless crystals melting at 234°-236° C(decomposition with foaming).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04085116 |
| Source dataset | uspto-grants-1978_04 |
| ORD ID | ord-a6ec4525eedd44c297b9810ecf1ab685 |
| Source note | uspto-grants-1978_04 |