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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1450735Erstellt: 26. Oktober 2026

Chloroform → 1-oxoheptyl-D-allo-Threonine

https://huagongshe.com/reaction/1450735

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroformHCID 6212—
EduktSodium HydroxideHCID 14798—
EduktHeptanoyl chlorideHCID 17313—
EduktD-AllothreonineHCID 90624—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-oxoheptyl-D-allo-ThreonineHCID 22851676—

Reaktionsschritte

A solution of n-heptanoyl chloride (440 mL, 2.83 mmol) in THF (250 mL) is added dropwise, over a period of 30 min, to a cold (-5° to 0° C.), vigorously stirred mixture of D-allo-Thr (300 mg, 2.51 mmol) and 2N aq. NaOH (3.5 mL, 7.0 meq) in THF (4.0 mL). The resulting mixture is stirred for 2 h at the same temperature and overnight at room temperature. The volatiles are removed and the residue is diluted with water and acidified, using conc. HCl. The mixture is extracted with EtOAc and the combined organic solution is washed with brine, dried, filtered, and concentrated to provide crude 2c-1 (420 mg, containing 10% excess heptanoyl reagent) which solidifies upon standing. NMR δ1.28 (d, J=6.5, 3 H), 4.20 (m, 1H), 4.61 (dd, J=3.4, 6.6, 1H), 6.56 (br d, J=6.9, 1H); [α]D26 -38±2 (CHCl3).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05602275
Quelldatensatzuspto-grants-1997_02
ORD IDord-4a049bcd42fa499e8f2fa5b49e702ff0
Quellennotizuspto-grants-1997_02