HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616984Generated: October 29, 2026
Borane;tetrahydrofuran → N-Dodecyl-4-ethoxyaniline
https://huagongshe.com/reaction/616984
Participants
| Role | Name | HCID | Charge |
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| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | HCID 20367077 | HCID 20367077 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | N-Dodecyl-4-ethoxyaniline | HCID 20367071 | 75% |
Reaction Steps
N-dodecanoyl-p-ethoxyaminobenzene (6g, 0.019 mole) was placed in a 250 ml round-bottom flask with Borane/THF complex (50 ml, 1M solution in tetrahydrofuran, stabilized with 5 mole percent sodium borohydride). The flask was flushed with nitrogen, stoppered with a drierite tube and allowed to stand at room temperature for 20 hours. Water was then added slowly to react with excess diborane. Formation of the amine salt was avoided by refluxing the reaction mixture with triethylamine (5 ml) for one hour. The mixture was cooled and the layers separated. The upper layer was washed with water (3 × 20 ml). A fourth wash emulsified the mixture. It was broken by addition of salt. The upper layer was dried with anh. sodium sulphate and evaporated to dryness yielding 5.56g (97%) of white plates of crude product. Crystallization from methanol afforded 4.3g (75%) of N-dodecyl-p-ethoxy-aminobenzene in the form of white plates, m.p. 38°-39° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04076849 |
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| Source dataset | uspto-grants-1978_02 |
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| ORD ID | ord-2b50086c7e2a4fefb260e95c82370b9f |
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| Source note | uspto-grants-1978_02 |
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