Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052314Generated: November 3, 2026

Acetic Acid → 6-((4-(Prop-2-yn-1-yloxy)benzyl)amino)hexanoic acid

https://huagongshe.com/reaction/1052314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant6-Aminohexanoic AcidHCID 564—
Reactant4-(Propargyloxy)benzaldehydeHCID 1897533—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
Product6-((4-(Prop-2-yn-1-yloxy)benzyl)amino)hexanoic acidHCID 86676471—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 6-aminohexanoic acid (2.62 g, 20 mmol), 4-(prop-2-yn-1-yloxy)benzaldehyde (0.80 g, 5.0 mmol) and acetic acid (0.50 mL) in DCE (50 mL) was heated at 80° C. for 60 min. The reaction mixture was cooled to 0° C., and treated with NaBH(OAc)3 (2.11 g, 10 mmol). The reaction was stirred at room temperature for 12 hours and decomposed with water and then extracted with DCM. The organic layer was dried and concentrated under reduced pressure to give a residue, which was purified using a Biotage SP4 and gradient elution of 5-50% methanol in DCM. The yield of the target compound 6-((4-(prop-2-yn-1-yloxy)benzyl)amino)hexanoic acid was 62% (0.856 g). 1H NMR (400 MHz, DMSO-d6): δ 7.19 (d, J=8.4 Hz, 2H), 6.86 (d, J=8.4 Hz, 2H), 4.71 (s, 2H), 3.56 (s, 2H), 3.49 (s, 1H), 2.39 (t, J=7.0 Hz, 2H), 2.00 (t, J=7.2 Hz, 2H), 1.41-1.19 (m, 6H); MS (ESI), 276.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388144B2
Source datasetuspto-grants-2016_07
ORD IDord-50f2d53bc4b6499db8c2f7b5ab60c96f
Source noteuspto-grants-2016_07