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HRID 276287Erstellt: 24. Oktober 2026

1,3-Dichloro-2-isothiocyanatobenzene → HCID 18316179, Verbindung

https://huagongshe.com/de/reaction/276287

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3-Dichloro-2-isothiocyanatobenzeneHCID 123239—
EduktN-Cyclohexyl-1,1-dimethyl-2-hydroxyethanamineHCID 277599—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-Cyclohexyl-1,1-dimethyl-2-hydroxyethanamineHCID 277599—
ProduktHCID 18316179HCID 1831617965,3%

Reaktionsschritte

N-Cyclohexyl-1,1-dimethyl-2-hydroxyethanamine was prepared in a manner analogous to Method B4a. A solution of 2,6-dichlorophenyl isothiocyanate (1.2 g, 6.0 mmol) and N-cyclohexyl-1,1-dimethyl-2-hydroxyethanamine (1.0 g, 6.0 mmol) in CH2Cl2 (10 mL) was stirred for 20 h at room temp. The resulting mixture was concentrated under reduced pressure, then treated with a 33% HCl solution (15 mL). The resulting mixture was heated at the reflux temp. for 1 h, cooled to room temp. and neutralized with a 45% NaOH solution. The resulting slurry was filtered, and the resulting solids were washed with water (20 mL), then recrystallized (EtOH) to yield 2-(2,6-dichlorophenylimino)-3-cyclohexyl-4,4-dimethyl-1,3-thiazolidine (0.70 g, 33%/o): mp 134° C. When appropriate, the product was converted into the HCl salt by dissolving the free base (5 mmol) in Et2O (50 mL) and treating this solution with a 2N ethereal HCl solution until no more solid precipitated. The resulting slurry was filtered and the resulting solids were washed with Et2O (25 mL) followed by EtOAc (25 mL).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06353006B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-c9c145cf06f64feabc107217a566f25c
Quellennotizuspto-grants-2002_03