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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829719Generated: November 4, 2026

Tetrahydrofuran → HCID 22054689, compound

https://huagongshe.com/reaction/1829719

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium ThiosulfateHCID 24477—
ReactantHCID 68883160HCID 68883160—
CatalystOsmium TetroxideHCID 30318—
SolventWaterHCID 962—
ProductHCID 22054689HCID 22054689—

Reaction Steps

To a stirred slurry of N-[2-(3,4-dichlorophenyl)-4-pentenylbutyl]-N-[(carboxymethyl)methyl]-3-cyano-2-ethyl-1-naphthamide (0.51 g) and NaIO4 (0.47 g) in 100 mL 1:1 THF:H2O was slowly added 0.32 mL OsO4 solution (4% w/w in H2O). Mixture was stirred for 18 h, 10 mL sat'd Na2S2O3(aq) was added, THF was evaporated, and aqueous residue was extracted with DCM. Extracts were dried over Na2SO4, filtered, and concentrated. This gave 0.64 g of N-[2-(3,4-dichlorophenyl)-4-oxobutyl]-N-[(carboxymethyl)methyl]-3-cyano-1-naphthamide after purification by chromatography (100:1, DCM:MeOH); MS: m/z 511 (M+); 1H NMR (CDCl3) δ 9.53 (s), 8.25 (s), 7.79 (d), 7.70-7.20 (m), 6.89 (d), 6.73 (d), 6.48 (dd), 4.58-4.20 (m), 3.88 (s), 3.84 (s), 3.60-3.21 (m), 3.18-2.82 (m), 2.65-2.32 (m), 1.33 (t).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07064136B2
Source datasetuspto-grants-2006_06
ORD IDord-b3c9383f303b494a9540381a215255ec
Source noteuspto-grants-2006_06