HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033134Generated: November 2, 2026
Acetic Acid → N-(4'-iodophenyl)-2-aminooctane
https://huagongshe.com/reaction/1033134
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | 2-Octanone | HCID 8093 | — |
| Reactant | 4-Iodoaniline | HCID 10893 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Product | N-(4'-iodophenyl)-2-aminooctane | HCID 9927521 | 88.2% |
Reaction Steps
A flask containing 4-iodoaniline (11.0 g, 50.2 mmol) was charged with dry dichloroethane (125 ml), 2-octanone (7.9 ml, 50.0 mmol) and sodium triacetoxyborohydride (13.8 g, 65 mmol). After stirring for 10 minutes, acetic acid (2.9 ml, 50.7 mmol) was added via syringe over a 5 minute period. The reaction was stirred under an N2 atmosphere for 16 hrs. At the end of this period the reaction was quenched by the careful addition of a solution of saturated aqueous ammonium chloride (100 ml). After stirring for 0.5 hr, the reaction was poured over ether (250 ml) and the layers were separated. The ether layer was washed with saturated aqueous ammonium chloride (100 ml), dried (Na2SO4), filtered and evaporated in vacuo. Flash column chromatography (silica, 1:39; EtOAC:hexanes) provided N-(4'-iodophenyl)-2-amino octane (14.6 g, 88%) as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05310537 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-d41a4156190449f8b1ce9f4d061913d3 |
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| Source note | uspto-grants-1994_05 |
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