HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417759Generated: October 25, 2026
Triethylamine → 3-(Biotinamido)butyric acid
https://huagongshe.com/reaction/417759
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Beta-Aminobutyric Acid | HCID 10932 | — |
| Reactant | HCID 20610691 | HCID 20610691 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(Biotinamido)butyric acid | HCID 87090959 | 98% |
Reaction Steps
Preparation was accomplished as described by Wilbur [Bioconj. Chem. 1997, 8, 572]. To a 0.13 g (1.3 mmol) quantity of 3-aminobutyric acid dissolved in 20 mL of DMF under argon atmosphere was added 0.4 mL (2.5 mmol) of triethylamine followed by 0.5 g (1.3 mmol) of biotin tetrafluorophenyl ester. The reaction was stirred at 25° C. for 24 h and the solvent was removed under vacuum. The residue was triturated with acetonitrile and filtered. The isolated solid was dried under vacuum to yield 0.5 g (98%) of product as a colorless solid, mp 161-163° C. 1H NMR (DMSO-d6): O 7.6 (m, 1H), 6.2 (d, J=11.2 Hz, 2H), 3.9-4.2 (m, 3H), 2.6 (m, 2H), 2.35 (d, J=12.6 Hz, 1H), 1.7-2.1 (m, 4H), 0.7-1.5 (m, 10H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08092782B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-5e7a11f46e2c4c7983ef69aa021968b7 |
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| Source note | uspto-grants-2012_01 |
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