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HCID 4147229, compound → N-Heptyloctan-1-amine

HRID 128297
Notes
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Reaction equation

HRID 128297 reaction equation
[CH2:1]([NH:9][C:10]([CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])=O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].B#B>O1CCCC1>[CH2:10]([NH:9][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17]
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 4147229HCID 4147229, compoundHCID 6328200Diboron

Product 1

HCID 12905714N-Heptyloctan-1-amine

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

Octylamine was acrylated with one equivalent of heptanoyl chloride to provide N-octylhexanecarboxamide. The amide was reduced by reaction with diborane in tetrahydrofuran to provide N-heptyloctylamine. To a cold stirred solution of 19.79 g. of N-heptyloctylamine and 23.4 g. of sodium carbonate in 82 ml. of acetone and 82 ml. of water was added dropwise over thirty minutes a solution of 13.7 ml. of acetyl chloride in 164 ml. of acetone. The reaction mixture was stirred for twelve hours following complete addition, after which time the solvent was removed by evaporation under reduced pressure. The residual oil was dissolved in diethyl ether and washed with water and with 2 N hydrochloric acid. The ethereal solution then was dried and the solvent was removed by evaporation to provide 22.48 g. of N-heptyl-N-octylacetamide.

Sources & evidence

ORD record
ord-1a186d2afe164ab08ec961251afd5e78
Source dataset
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04259354

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes