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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900063Generated: October 26, 2026

Isobutyl Acetate → Mycophenolate Mofetil

https://huagongshe.com/reaction/900063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyl AcetateHCID 8038—
Reactant2-MorpholinoethanolHCID 61163—
ReactantStannous chloride dihydrateHCID 61436—
ReactantMycophenolic AcidHCID 446541—
ProductMycophenolate MofetilHCID 5281078—

Reaction Steps

A mixture of mycophenolic acid (192 g, 0.6 mol) and 4-(2-hydroxyethyl)-morpholine (440 ml, 6 molar equivalents) was stirred at 150-155° C. for 4 hours in the presence of tin(II) chloride dihydrate (20.4 g, 0.15 molar equivalents) under nitrogen atmosphere. After the completion of the reaction, the reaction mixture was allowed to cool to room temperature. The obtained dark liquid was poured into isobutyl acetate (4.0 l). The solution was extracted with 2% of aqueous sodium bicarbonate solution (1.2 l, then 2×0.4 l). After the first addition of sodium bicarbonate solution the formed two-phase system was treated with charcoal (40 g) and filtrated (an emulsion was filtered off). The solution was extracted with water (1 l). -After phase separation the organic phase was washed with water (1 l) and evaporated to dryness at 40-50° C. under vacuum. To the solid material acetone (400 ml) and isopropanol (3.8 l) were added and the mixture was warmed to 40-45° C. (the material was dissolved). The solution was cooled to −5° C. during 6 hours and it was stirred at this temperature for 10-12 hours. After filtration, the crystals were washed with 2:19 acetone/isopropanol mixture (420 ml). The crude compound was dried in vacuum at 60° C. The yield was 169-195 g (65-75%). HPLC impurity profile: MPA=0.1%. Assay: 99.85%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07358247B2
Source datasetuspto-grants-2008_04
ORD IDord-7dd091eca18d4124b5ee7bd8e76176fb
Source noteuspto-grants-2008_04