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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 74972Erstellt: 24. Oktober 2026

Triethylamine → benzyl (1S,3R)-3-(4-chlorobutanamido)cyclohexylcarbamate

https://huagongshe.com/de/reaction/74972

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt4-Chlorobutyryl chlorideHCID 78370—
EduktBenzyl ((1S,3R)-3-aminocyclohexyl)carbamateHCID 69756715—
LösungsmittelDichloromethaneHCID 6344—
Produktbenzyl (1S,3R)-3-(4-chlorobutanamido)cyclohexylcarbamateHCID 68101865—

Reaktionsschritte

To a stirred slurry of benzyl N-[(1S,3R)-3-aminocyclohexyl]carbamate, 18e, (0.97 g, 3.41 mmol) in CH2Cl2 (34 mL), was added Et3N (1.00 mL, 7.15 mmol), followed by 4-chlorobutanoyl chloride (0.40 mL, 3.58 mmol). After stirring at room temperature, the mixture was diluted with CH2Cl2, washed with 1N HCl (2×), 1N NaOH (2×), and brine. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo to give 1.07 g of the desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08829007B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-33806c5de7e74f21baa2a380cd0f178b
Quellennotizuspto-grants-2014_09