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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 407151Erstellt: 25. Oktober 2026

1-Hydroxybenzotriazole → Boc-Beta-Ala-OSu

https://huagongshe.com/reaction/407151

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-HydroxybenzotriazoleHCID 75771—
EduktN-((1,1-dimethylethoxy)carbonyl)-beta-alanineHCID 76809—
EduktN-HydroxysuccinimideHCID 80170—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
LösungsmittelDimethylformamideHCID 6228—
ProduktBoc-Beta-Ala-OSuHCID 1068459972.634.728%

Reaktionsschritte

A mixture of N-Boc-β-Ala-OH (1 g, 5.29 nmol), N-hydroxysuccinimide (0.9 g, 7.82 mmol) in DMF (10 mL) were added HOBt (0.7 g, 5.25 mmol) and EDCI.HCl (1 g, 5.23 mmol) at 5° C. The reaction mixture was warmed to RT and stirred for 16 h. The progress of the reaction was monitored by TLC. The reaction was quenched with water and extracted with ethyl acetate (2×150 mL). The combined organic layers were washed with water (3×100 mL), brine (150 mL), dried over anhydrous Na2SO4 and concentrated under reduced pressure. The crude compound was triturated with ether (2×25 mL) to afford N-Boc-β-Ala-OSu (1.1 g, crude) as white solid. 1H NMR (500 MHz, CDCl3): δ 5.10 (bs, 1H), 3.52 (q, J=6.0 Hz, 2H), 2.85-2.82 (m, 6H), 1.31 (s, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754227B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-da67826d218046bd93cebe57526ab382
Quellennotizuspto-grants-2014_06