Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589654Generated: October 26, 2026

Methanol → Meropenem trihydrate

https://huagongshe.com/reaction/589654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDichloromethaneHCID 6344—
ReactantMeropenemHCID 441130—
ReactantMonobasic potassium phosphateHCID 516951—
CatalystZincHCID 23994—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductMeropenem trihydrateHCID 441129—

Reaction Conditions

Temperature27 °C

Reaction Steps

20 g of meropenem-PNB was dissolved in 200 mL of tetrahydrofuran. 60 g of potassium phosphate monobasic (KH2PO4) dissolved in 400 mL of water was added thereto and heated to 27° C. 80 g of zinc powder was slowly added portionwise and stirred between 25 to 35° C. for 1 hour. After the completion of the reaction was confirmed, 220 mL of methylene chloride was added and stirred for 10 minutes, and then filtered to remove zinc powder. The aqueous layer was separated and washed 2 times with 100 mL of methylene chloride, by which tetrahydrofuran present in the aqueous layer was removed completely. The aqueous layer was cooled and developed in a column filled with adsorption resin SP-207 for adsorption. The resin column was washed with 2 L of water to remove potassium phosphate salt used in the reaction and impurities, and developed with 2 L of 60% methanol to elute meropenem completely. The fractions containing meropenem were collected and a buffer solution of N-methylmorpholine/acetic acid (pH 6.5) was added thereto, and concentration was conducted to a volume 10 times greater than the weight of meropenem-PNB. 1100 mL of acetone was added to generate crystal and stirred at room temperature for 1 hour. After filtration and drying, 9.78 g of meropenem trihydrate was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233963B2
Source datasetuspto-grants-2016_01
ORD IDord-e631d673e2df43378ae2fcc514566dbc
Source noteuspto-grants-2016_01