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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973871Generated: October 30, 2026

Hydrochloric Acid → HCID 12242169, compound

https://huagongshe.com/reaction/973871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
Reactant2,5-Furandione, 3-methoxy-4-methyl-HCID 10290846—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12242169HCID 12242169—

Reaction Steps

2-Methoxy-3-methylmaleic anhydride (9 g), (M. M. Kayser et al, Can.J.Chem., 1986, 64, 104) in dry THF (50 mls) was added, dropwise to a suspension of sodium borohydride (1.5 g) in THF (200 mls) at 0°-5° C., over ca 30 mins. The reaction mixture was allowed to warm to room temperature for a further 30 mins. T.l.c. analysis showed no remaining starting material. The solution was carefully neutralized with 5M aqueous hydrochloric acid and then the THF removed in vacuo. The aqueous solution was extracted with ethyl acetate washed with brine and dried. After removal of solvent the crude material was purified by `flash` chromatography on silica gel eluting with 50% ethyl acetate/hexane. The title compound was obtained as a colourless crystalline solid, (6.683 g, 73%), m.p. 79° C., benzene. νmax (CH2Cl2) 3540(w), 3300 (br), 1755, 1670, 1455, 1380 and 1325cm- ; δH (CDCl 3) 1.78 (3H, s), 4.06 (3H, s), 5.96 (1H, br.s, sharpens on D2O shake) and 6.23 (1H, br.s, exch).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05064649
Source datasetuspto-grants-1991_11
ORD IDord-35def3c0f7394c13b19021ab2a1ed88d
Source noteuspto-grants-1991_11