HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminobutanal → 4-Dibutylaminobutyraldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminobutanal | HCID 118 | — |
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Dibutylaminobutyraldehyde | HCID 18944389 | 39% |
Reaction Steps
A! A solution of 4-aminobutyraldehyde diethylacetale (90 ml, 0.5 mole) and butyl bromide (121 ml, 1.1 mole) in ethanol (1.000 ml) was added with a 1N solution of sodium hydroxide (1.130 ml). The reaction mixture was refluxed for 8 hours. The reaction solvent was evaporated off and the aqueous solution was extracted with diethyl ether. The organic phases were combined and anhydrified over sodium sulfate, then evaporated under vacuum. The resulting crude was purified by fractionated distillation to yield 54 g of 4-dibutylaminobutyraldehyde diethylacetale (yield: 39%). B.p.: 95°-06° C. (0,05 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05827881 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-ff738e2080e34a5382cf0f8aad79fbd6 |
| Source note | uspto-grants-1998_10 |