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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595869Generated: October 30, 2026

Ethyl Acetate → HCID 53922974, compound

https://huagongshe.com/reaction/1595869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 7-bromoheptanoateHCID 122490—
ReactantHCID 22246767HCID 22246767—
SolventDimethylformamideHCID 6228—
ProductHCID 53922974HCID 53922974—

Reaction Steps

A solution of NaH (60% in oil, 338 mg, 8.45 mmol) in DMF (23 mL) was cooled to 0° C. followed by addition of N-[2-(3,5-dichloro-phenoxy)-ethyl]-methanesulfonamide (2.0 g, 7.04 mmol). The reaction was stirred at room temperature for 0.5 h and was cooled to 0° C. followed by addition of ethyl 7-bromoheptanoate (2.0 g, 8.45 mmol). The reaction was heated at 65° C. for 3 h and was cooled to room temperature. EtOAc was added and the organic solution was washed consecutively with 1 N HCl, water, and brine. The organic solution was dried (MgSO4), filtered, and concentrated. Purification by flash chromatography (4:1 hexanes:EtOAc) provided the title compound (2.84 9). 1HNMR (400 MHz, CDCl3) δ 6.95 (m, 1H), 6.75 (m, 2H), 4.06 (m, 5H), 3.56 (t, 2H), 3.22 (t, 2H), 2.86 (s, (t, 2H), 1.60 (m, 4H), 1.32 (m, 4H), 1.22 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288120B1
Source datasetuspto-grants-2001_09
ORD IDord-103d8b670a95494f93927c9bcfddf73e
Source noteuspto-grants-2001_09