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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551753Generated: October 25, 2026

7-Tridecanone → Tridecan-7-amine

https://huagongshe.com/reaction/551753

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-TridecanoneHCID 10015—
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
ProductTridecan-7-amineHCID 574991116.1%

Reaction Steps

In a 250 mL round bottom flask, 5.00 g (25.5 mmol) dihexylketone, 19.7 g (255 mmol) ammonium acetate, and 1.10 g (17.8 mmol) sodium cyanoborohydride (NaBH3CN) were dissolved in 75 mL absolute MeOH and stirred at room temperature for 48 hours, until no significant amount of the starting material could be detected by NMR. The mixture was quenched by adding concentrated hydrochloric acid (HCl) dropwise (˜3 mL), then concentrated in vacuo. The resulting white solid was taken up in 500 mL water, basified to pH 10 with solid potassium hydroxide (KOH), and extracted with chloroform (CHCl3) twice (200 mL each). The CHCl3 fractions were combined and concentrated to give 4.12 g (81%) of 1-hexylheptylamine 1 as a pale yellow oil. 1H NMR (D2O, 500 MHz): δ 0.73 (t, 6H), 1.15-1.23 (m, 16H), 1.55 (m, 4H), 3.13 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947837B2
Source datasetuspto-grants-2011_05
ORD IDord-e5cf9284ca1c4c96bef0ce33f5efeb1d
Source noteuspto-grants-2011_05