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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211430Generated: November 1, 2026

Sodium Chloride → HCID 53639899, compound

https://huagongshe.com/reaction/2211430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant(S)-2-(2-Methoxyphenyl)propanoic acidHCID 11137716—
ReactantHCID 57191444HCID 57191444—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 53639899HCID 5363989958.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

30 mg of 1-hydroxybenzotriazole hydrate, 0.66 g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide and 0.6 cm3 of diisopropylethylamine are added to a solution of 1.1 g of (3aS,4S,5S,7aS)-7,7-diphenyl-4-(2-methoxyphenyl)-perhydroisoindole-4,5 -diol and 0.58 g of (S)-2-(2-methoxyphenyl)-propanoic acid in 30 cm3 of methylene chloride, cooled to 0° C. The mixture is stirred at room temperature for 3 hours and 30 minutes and 100 cm3 of water and 50 cm3 of an aqueous saturated solution of sodium chloride are added. The organic phase is decanted, dried over magnesium sulphate and concentrated to dryness under reduced pressure (2.7 kPa). The yellow residue obtained is chromatographed over a Merck silica gel column (particle size 0.04-0.06 mm, diameter 2 cm, height 30 cm) by eluting under a pressure of 0.5 bar of nitrogen with a mixture of cyclohexane and ethyl acetate (60/40 by volume) and collecting fractions of 25 cm3. Fractions 6 to 14 are combined and then concentrated to dryness under reduced pressure (2.7 kPa). 0.9 g of (3aS,4S,5S,7aS)-7,7-diphenyl-4-(2-methoxyphenyl)-2-[2-(2-methoxyphenyl)-(S)-propionyl]-perhydroisoindole-4,5-diol which melts at 256° C. is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05463077
Source datasetuspto-grants-1995_10
ORD IDord-a3c2b796bd404a099d978ee491bb42fd
Source noteuspto-grants-1995_10