HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 13071121, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 15629417 | HCID 15629417 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13071121 | HCID 13071121 | — |
Reaction Steps
A solution of 340 mg of 2,5,11-trioxatricyclo[4,3,1,14,8 ] undecan-3-one of the formula Ia in 10 ml of absolute ethanol is treated at room temperature with 150 mg of sodium borohydride and the mixture is stirred for 2 hours. The reaction mixture is diluted with 10 ml of water, the pH adjusted to 8 with a few drops of glacial acetic acid and the resulting solution is concentrated under reduced pressure to about 3 ml. The concentrate is extracted three times with altogether 100 ml of methylene chloride, the combined extracts are dried with sodium sulphate and the solvent is distilled off to give 3-hydroxymethyl-2,4-dioxabicyclo[3,3,1]nonan-7-ol of the formula IIa, which melts at 146°-149°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03941813 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-c2c7d52f70d64d37b823df4616d71eb5 |
| Source note | uspto-grants-1976_03 |