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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 449503Erstellt: 25. Oktober 2026

3-Hydroxybenzaldehyde → Methyl 2-(tert-butoxycarbonylamino)-3-(3-hydroxyphenyl)acrylate

https://huagongshe.com/reaction/449503

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-HydroxybenzaldehydeHCID 101—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
EduktMethyl ((tert-butoxy(hydroxy)methylidene)amino)(dimethoxyphosphoryl)acetateHCID 397380—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl AcetateHCID 8857—
ProduktMethyl 2-(tert-butoxycarbonylamino)-3-(3-hydroxyphenyl)acrylateHCID 6754293696%

Reaktionsschritte

Methyl [(tert-butoxycarbonyl)amino](dimethoxyphosphoryl)acetate (Fluka, Cat. #09659) (0.97 g, 3.3 mmol) and 3-hydroxybenzaldehyde (0.400 g, 3.28 mmol) were combined in methylene chloride (14 mL) at r.t. under nitrogen. To this DBU (0.68 mL, 3.9 mmol) was added and the reaction was stirred at r.t. for 2 h. The reaction was taken up in ethyl acetate, washed with 1 N HCl, brine, dried over magnesium sulfate and concentrated under reduced pressure to give the crude product as an oil. The product was purified by Flash chromatography on a silica gel column eluting hexane: ethyl acetate gradient to give methyl 2-(tert-butoxycarbonylamino)-3-(3-hydroxyphenyl)acrylate (0.92 g, 96%) as a clear oil Analytical LCMS (M+H-Boc)+: m/z=193.9.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08481732B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-c0676be429e740f2b8ede788a3d1cdd5
Quellennotizuspto-grants-2013_07