| Identification | Back Directory | [Name]
1,1-Diethoxybutane | [CAS]
3658-95-5 | [Synonyms]
1,1-DIETHOXYBUTANE
Butane, 1,1-diethoxy-
Butanal diethyl acetal
butyraldehyde ethyl acetal
BUTRALDEHYDE DIETHYL ACETAL
Butylaldehyde diethyl acetal
BUTYRALDEHYDE DIETHYL ACETAL
n-Butyraldehyde diethyl acetal
BUTYRALDEHYDE DIETHYLACETAL, 97+% | [EINECS(EC#)]
222-913-5 | [Molecular Formula]
C8H18O2 | [MDL Number]
MFCD00038316 | [MOL File]
3658-95-5.mol | [Molecular Weight]
146.23 |
| Questions And Answer(Q&A) | Back Directory | [Preparation]
To a three-necked flask equipped with an air-tight mechanical stirrer, dropping funnel, reflux condenser, and drying tube, are added 3.0 gm (1.25 gm-atom) magnesium turnings, 50 ml of dry ether, and a small crystal of iodine. Then 5 gm of rt-butyl bromide is added dropwise until 171.0 gm (1.25 mole) has been added. The reaction takes about ½ - l h r if the reaction mixture is cooled. The solution is refluxed for ½ hr, cooled to 50°C, and then 148 gm (1.0 mole) of triethyl orthoformate is added dropwise over a ½-hr period. The reaction mixture is refluxed for 16 hr, crushed ice added to decompose the excess Grignard reagent, the ether separated and washed with water. The water layer is added to a separatory funnel containing 200 ml of ether, treated with acetic acid to pH 7.0, shaken, and the ether separated. The latter ether layer is washed with 10% aqueous sodium carbonate, water, and dried. The latter water layer is extracted twice again with ether (200 ml). The combined ether layers are dried over potassium carbonate and fractionated to afford 128 gm (80%), b.p. 143°-144°.
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