Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828111Generated: November 1, 2026

o-Fluorobenzaldehyde → HCID 22064650, compound

https://huagongshe.com/reaction/1828111

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-FluorobenzaldehydeHCID 67970—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 22064712HCID 22064712—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
ProductHCID 22064650HCID 2206465076%

Reaction Steps

(RS)-N-(2-amino-4-cyano-benzyl)-2-ethoxy-2-(4-fluoro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-acetamide (0.060 g) was treated in MeOH (1 ml) successively with 2-fluoro-benzaldehyde (56 mg) and 1 ml of a MeOH-solution containing scrupulously dried ZnCl2 (83 mg) and NaCNBH3 (29 mg). The reaction mixture was stirred for 6 h at 50–55° C., poured onto crashed ice and extracted two times with ethyl acetate. The combined organic layers were washed with water and brine and dried over magnesium sulfate. The solvent was removed under reduced pressure and the residue purified by column chromatography (silica gel, hexane/AcOEt=6/4) to yield (RS)-N-[4-cyano-2-(2-fluoro-benzylamino)-benzyl ]-2-ethoxy-2-(4-fluoro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-acetamide (58 mg) as yellow oil, MS 505.4 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056932B2
Source datasetuspto-grants-2006_06
ORD IDord-db8aa210a3b24b2eb7e2548c1e2f2400
Source noteuspto-grants-2006_06