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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876413Generated: October 29, 2026

Sodium hydride → 1-Tert-butyl 4-ethyl 4-fluoro-5-oxoazepane-1,4-dicarboxylate

https://huagongshe.com/reaction/876413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantSelectfluorHCID 2724933—
Reactant1-tert-Butyl 4-ethyl 5-oxoazepane-1,4-dicarboxylateHCID 4436570—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product1-Tert-butyl 4-ethyl 4-fluoro-5-oxoazepane-1,4-dicarboxylateHCID 6723384574.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

NaH (2.66 g, 105 mmol) was suspended in THF (300 mL) and cooled to 0° C., and 1-tert-butyl 4-ethyl 5-oxoazepane-1,4-dicarboxylate (30 g, 105 mmol) was added as THF solution (550 mL) using an addition funnel over 30 minutes. The mixture was stirred for 30 minutes and then diluted with DMF (200 mL). Selectfluor (41.0 g, 116 mmol) was added as a DMF solution (200 mL). The mixture was warmed to ambient temperature and stirred for 2 hours. The mixture was then concentrated to remove THF and diluted with 1N KHSO4 (300 mL), water (300 mL) and EtOAc (750 mL). The organic layer was washed with brine (2×250 mL). The combined aqueous layers were washed with EtOAc (200 mL) and this organic layer was washed with brine (200 mL). The combined organic layers were then dried over Na2SO4, filtered and concentrated. The crude product was passed through a silica gel plug (1 kg, 20 to 40% EtOAc/hexanes) to provide 23.6 g (74%) of the product as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987251B2
Source datasetuspto-grants-2015_03
ORD IDord-6911c5dfee16448994fa46c7ad128415
Source noteuspto-grants-2015_03