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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 239708Erstellt: 24. Oktober 2026

Cycloheptylamine → 3-(cycloheptylamino)propane-1-sulfonic Acid

https://huagongshe.com/de/reaction/239708

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCycloheptylamineHCID 2899—
EduktPropane sultoneHCID 14264—
EduktPotassium BromideHCID 253877—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(cycloheptylamino)propane-1-sulfonic AcidHCID 1118393872%

Reaktionsschritte

Cycloheptylamine (3.9 mL, 30 mmol) was added to a solution of 1,3-propane sultone (4.1 g, 33 mmol) in THF (65 mL). The mixture was heated at reflux for 5 hours with a heating mantle. The mixture was cooled to room temperature and the solid was collected by filtration, and then dried in a vacuum oven for 1 hour at 60° C. (6.21 g). The solid material was dissolved in methanol/water (30 mL/3 mL, v/v). The solution was cooled slowly to room temperature, and further cooled with an ice-bath. The solid product was collected by filtration, rinsed with methanol, air-dried for 15 minutes, and further dried in a vacuum oven at 60° C. Compound CK was obtained as small white flakes (5.08 g, 72% yield). m.p. 341-43° C. 1H NMR (500 MHz, D2O) δ 1.21-1.42 (m, 8H), 1.45-1.51 (m, 2H), 1.79-1.89 (m, 4H), 2.76 (7, J=7.3 Hz, 2H), 2.96 (t, J=7.8 Hz, 2H), 3.35 (m, J=4.6 Hz, 1H). 13C NMR (125 MHz, D2O) δ 21.6, 23.3, 27.3, 30.5, 43.6, 48.0, 59.6. FT-IR (KBr) νmax 2924, 1615, 1464, 1243.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642801B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-8e5fb6ddec9144a494daacf08e5656b4
Quellennotizuspto-grants-2014_02