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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377882Generated: October 26, 2026

3-(1,3-Benzodioxol-5-yl)prop-2-enoic acid → (S)-3-(3,4-Methylenedioxyphenyl)-prop-2-enoylproline benzyl ester

https://huagongshe.com/reaction/1377882

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(1,3-Benzodioxol-5-yl)prop-2-enoic acidHCID 16917—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantProline benzyl ester hydrochlorideHCID 2733413—
ReactantL-Alanine, phenylmethyl ester, hydrochloride (1:1)HCID 12210893—
SolventAcetonitrileHCID 6342—
Product(S)-3-(3,4-Methylenedioxyphenyl)-prop-2-enoylproline benzyl esterHCID 5412418374.9%

Reaction Steps

A solution of 192 mg (1.0 mmol) of 3,4-methylenedioxycinnamic acid, 121 mg (0.5 mmol) of proline benzyl ester hydrochloride and 108 mg (0.5 mmol) of alanine benzyl ester hydrochloride in 6 mL of acetonitrile was treated sequentially with 0.35 mL (2.0 mmol) of diisopropylethylamine and 443 mg (1.0 mmol) of benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate. The mixture was stirred for 16 hrs then concentrated in vacuo. The residue was dissolved in 10 mL of dichloromethane and poured into 3 volumes of diethyl ether. The mixture was washed sequentially with water, 10% potassium bisulfate solution, water, saturated sodium bicarbonate solution, water and saturated sodium chloride solution. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography, using a stepwise gradient of 30%, 35%, 40%, and 45% ethyl acetate in hexane as eluant. Ester (9) (142 mg) was obtained as a colorless oil, Rf=0.4 (40% ethyl acetate/hexane); HPLC, Rt 12.26; 1H NMR (300 MHz) consistent with structure. Ester (10) (162 mg) was obtained as a colorless oil; TLC, Rf =0.22 (40% ethyl acetate/hexane); HPLC, Rt 11.84 min; 1H NMR (300 MHz) consistent with structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665774
Source datasetuspto-grants-1997_09
ORD IDord-9db45696506b4828a64ff6f7e96486d1
Source noteuspto-grants-1997_09