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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874248Generated: October 30, 2026

4-Fluorobenzaldehyde → HCID 67071636, compound

https://huagongshe.com/reaction/874248

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 67071652HCID 67071652—
SolventSodium BicarbonateHCID 516892—
ProductHCID 67071636HCID 6707163699%

Reaction Steps

A suspension of Intermediate 1 (250 mg, 0.77 mmol) in aqueous 10% NaHCO3 solution was extracted with DCM (3×10 ml). The organic phase was dried over Na2SO4 and evaporated. The resulting solid was dissolved in DCM (10 ml), treated with 4-fluoro-benzaldehyde (0.090 ml, 0.85 mmol) and NaBH(OAc)3 (245 mg, 1.15 mmol) as described in Example 2, Step A, to give (±)-(E)-3-[1′-(4-fluoro-benzyl)-4-oxo-spiro(chromane-2,3′-pyrrolidine)-6-yl]-acrylic acid methyl ester (300 mg, 0.76 mmol, 99%) as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980877B2
Source datasetuspto-grants-2015_03
ORD IDord-24f69e9b3c7b43cb9ee6c9cf23a2980b
Source noteuspto-grants-2015_03