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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373401Generated: October 30, 2026

Acetic Acid → HCID 67902560, compound

https://huagongshe.com/reaction/373401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantSodium hydrideHCID 24758—
ReactantHCID 11075738HCID 11075738—
SolventDimethylformamideHCID 6228—
ProductHCID 67902560HCID 6790256018%

Reaction Conditions

Temperature5 °C

Reaction Steps

4.0 g (93 mmol) sodium hydride (55 percent in oil) was added in 10 portions in 2 hours at -10° C. under argon to a solution of 19 g (77 mmol) of (3aS, 6aR)-[(R)-(1-phenylethyl)]-dihydro-1H-furo-[3,4-d]-imidazol-2,4-(3H, 3aH)-dione and 9.42 g (120 mmol) of chloromethyl methyl ether in 200 ml of dried N,N-dimethylformamide. The reaction mixture was stirred at 5° C. for 2 hours and then at room temperature for another 2 hours. Then 2 ml of acetic acid was added. Then the mixture was evaporated to dryness. Then the residue was taken up in 50 ml of water and 100 ml of dichloromethane, the phases were separated and the aqueous phase was extracted 2 times with 100 ml of dichloromethane. The organic phases were dried over magnesium sulfate and concentrated. After chromatographing the oily residue over silica gel with 500 ml of dichloromethane/ethyl acetate and concentrations of the fractions, 4.0 g (18 percent) of the title product was obtained as white powder. Concerning the product: Melting point: 96°-98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05162540
Source datasetuspto-grants-1992_11
ORD IDord-67de57fc5e094b82bf872f3a2df105a6
Source noteuspto-grants-1992_11