HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dihydroxybenzaldehyde → HCID 22164153, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dihydroxybenzaldehyde | HCID 90579 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 15058684 | HCID 15058684 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22164153 | HCID 22164153 | 89.4% |
Reaction Steps
Under a dry nitrogen atmosphere a mixture of 6.0 grams (0.026 mole) of 2,3-di(2-fluoroethoxy)benzaldehyde (prepared by the method of Example 1 from 2,3-dihydroxybenzaldehyde) and 1.3 gram (0.034 mole) of sodium borohydride in 130 ml of ethanol was stirred at room temperature for approximately 18 hours. The reaction was quenched with dilute hydrochloric acid, and the mixture was extracted with diethyl ether. The extract was washed with dilute hydrochloric acid followed by an aqueous, saturated sodium chloride solution. The organic phase was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure to yield 5.4 grams of 1,2-di-(2-fluoroethoxy)-3-hydroxymethylbenzene as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04960884 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-0f77282acf3d44e48b67862c62af58d7 |
| Source note | uspto-grants-1990_10 |