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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130388Generated: October 30, 2026

Sodium Bicarbonate → HCID 86586521, compound

https://huagongshe.com/reaction/130388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86586347HCID 86586347—
SolventEthyl AcetateHCID 8857—
ProductHCID 86586521HCID 86586521—

Reaction Steps

10.0 g (24.0 mmole) of {(2R)-7-nitro-8-[1-propenyl]-2,3-dihydro-1,4-benzo-dioxin-2-yl}methyl 4-methylbenzenesulfonate and 28.0 g (123 mmole) of stannous chloride dihydrate were combined and heated to 70° C. in ethyl acetate (250 mL) for 6 hours under nitrogen. After cooling to room temperature, the reaction mixture was poured into ice and was made basic with sodium bicarbonate. It was then extracted with ethyl acetate, washed with brine, dried over magnesium sulfate, filtered and evaporated to a brown oil. The crude oil was then chromatographed on silica gel with 50% hexane/methylene chloride to remove impurities and the desired product was eluted with 0.5% methanol/CH2Cl2 to give 8.16 g (91%) of the (R)-enantiomer of the title compound as a yellow oil. For analytical purposes, 50 mg of the yellow oil was crystallized from ethanol with the addition of fumaric acid to give the fumarate of the title compound. MS (ESI) m/z 375 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381723B2
Source datasetuspto-grants-2008_06
ORD IDord-cad44901627f462f840cb66105a4ee27
Source noteuspto-grants-2008_06