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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13952Erstellt: 24. Oktober 2026

Hydrochloric Acid → (+/-)-3-(5-Chloro-2-hydroxy-3-methoxyphenyl)-2-hydroxypropyl 4-methylbenzenesulfonate

https://huagongshe.com/de/reaction/13952

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt4-Toluenesulfonyl chlorideHCID 7397—
Eduktp-ToluenesulfonateHCID 85570—
Edukt(+/-)-3-[2-(Benzyloxy)-5-chloro-3-methoxyphenyl]-1,2-propanediolHCID 68583190—
Edukt(+/-)-3-[2-(Benzyloxy)-5-chloro-3-methoxyphenyl]-2-hydroxypropyl 4-methylbenzenesulfonateHCID 86598564—
KatalysatorPalladiumHCID 23938—
LösungsmittelPyridineHCID 1049—
Produkt(+/-)-3-(5-Chloro-2-hydroxy-3-methoxyphenyl)-2-hydroxypropyl 4-methylbenzenesulfonateHCID 86598563—

Reaktionsschritte

Treatment of (±)-3-[2-(benzyloxy)-5-chloro-3-methoxyphenyl]propane-1,2-diol (32.28 g, 0.1 mol) with p-toluenesulfonyl chloride (21 g, 0.11 mol) in pyridine (1000 mL) generally according to the procedure described for Intermediate 18 provided (±)-3-[2-(benzyloxy)-5-chloro-3-methoxyphenyl]-2-hydroxypropyl 4-methylbenzenesulfonate. Treatment of the tosylate with palladium on carbon (5 wt. %, 2.32 g) and hydrogen chloride (19 mL, 4.0 M in isopropanol) generally according to the procedure described for Intermediate 4 gave (±)-3-(5-chloro-2-hydroxy-3-methoxyphenyl)-2-hydroxypropyl 4-methylbenzenesulfonate. Treatment of the phenyl with triphenylphosphine (23.6 g, 0.09 mol) and diisopropyl azodicarboxylate (18.2 g, 0.09 mol) generally according to the procedure described for Intermediate 5 gave 28.2 g (76%) of (±)-(5-chloro-7-methoxy-2,3-dihydro-1-benzofuran-2-yl)methyl 4-methylbenzenesulfonate as a pale yellow solid. mp 99-102° C.; Anal. calcd. for C17H17ClO5S: C, 55.36; H, 4.65. Found: C, 55.35; H, 4.62.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728155B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-cdf570fc775b4f2c9c57bd8de576ce98
Quellennotizuspto-grants-2010_06