2-Aminoheptane → HCID 57244436, compound

HRID 1198725Notes

Reaction equation

C([C:5]1[CH:13]=[CH:12][C:8]([C:9](Cl)=O)=[CH:7][CH:6]=1)(C)(C)C.[NH2:14][CH:15]([CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])[CH3:16]>>[C:8]([N:14]([CH2:9][C:8]1[CH:7]=[CH:6][CH:5]=[CH:13][CH:12]=1)[CH:15]([CH3:16])[CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])([CH3:12])([CH3:9])[CH3:7]

Participants

Reactant 2

HCID 56032-Aminoheptane

HCID 743724-tert-Butylbenzoyl chloride

Product 1

HCID 57244436HCID 57244436, compound

Procedure

The N-t-butylbenzyl-N-(1-methylhexyl)amine was synthesized in the same manner as in Example 2, procedures 1 and 2 using 4-t-butylbenzoyl chloride and 2-aminoheptane as starting materials.

Sources & evidence

ORD record: ord-f593cdd53a844701b9975cf568299a79
Source dataset: uspto-grants-1994_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05281714

Reaction notes

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