HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Butanediol → 4-(2,2-Diethoxyethoxy)butanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Butanediol | HCID 8064 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(2,2-Diethoxyethoxy)butanol | HCID 18430111 | 41.9% |
Reaction Steps
To a mixture of 56.3 g of 1,4-butanediol and 400 ml of N,N-dimethylformamide was slowly added 11.0 g of 60% sodium hydride (in oil) with stirring under ice cooling. After stirring at room temperature for 12 hours, 49.3 g of bromoacetaldehyde diethylacetal was added dropwise to the reaction mixture, which was stirred at 60° C. for 8 hours. The reaction mixture was poured into ice water and extracted twice with ethyl acetate. The ethyl acetate layers were combined, washed with water, dried over magnesium sulfate and then concentrated to give a crude product. The crude product was subjected to silica gel chromatography, which afforded 21.6 g of 4-(2,2-diethoxyethoxy)butanol (yield, 41%), nD23.2 1.4314.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06140274 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-d5fdb1f5492b44dc824cda1ab4cdee9d |
| Source note | uspto-grants-2000_10 |