HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422506Generated: November 2, 2026
Acetic Acid → 6-((4-(Prop-2-yn-1-yloxy)benzyl)amino)hexanoic acid
https://huagongshe.com/reaction/1422506
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 6-Aminohexanoic Acid | HCID 564 | — |
| Reactant | 4-(Propargyloxy)benzaldehyde | HCID 1897533 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-((4-(Prop-2-yn-1-yloxy)benzyl)amino)hexanoic acid | HCID 86676471 | — |
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 644-(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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08926944B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-95a9e0170753421fa1937b576446c3b9 |
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| Source note | uspto-grants-2015_01 |
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