Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2335Generated: October 29, 2026

Sodium hydride → Methyl 3-(2-oxopiperidin-1-yl)benzoate

https://huagongshe.com/reaction/2335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantMethyl 3-(5-bromopentanoylamino)benzoateHCID 10686692—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-(2-oxopiperidin-1-yl)benzoateHCID 1068113556.2%

Reaction Steps

The bromide of Example 36 (1.50 g, 4.88 mmol) was taken up in dry DMF (40 ml) and treated with NaH (160 mg, 80% disp. in oil) at 0° C. The mixture was stirred at r.t. under nitrogen for 10 min, then KI (80 mg) added and the mixture heated at 70° C. for 4 h. The mixture was evaporated and partitioned between EtOAc and 1M HCl. The organic portion was washed with 5% KHCO3 and brine, filtered (Whatman® 1 PS, phase separator) and evaporated. The residue was chromatographed (eluant 2% MeOH in EtOAc) to provide a colourless oil (640 mg, 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728829
Source datasetuspto-grants-1998_03
ORD IDord-39e2a12366cc4afaa1054c2e96602afd
Source noteuspto-grants-1998_03