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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965276Generated: October 31, 2026

Hydrochloric Acid → 2-Nitro-4-t-butoxycarbonyl-benzoylfluoride

https://huagongshe.com/reaction/965276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantCyanuric fluorideHCID 12664—
ReactantSodium HydroxideHCID 14798—
ReactantTert-butyl 4-(methoxycarbonyl)-3-nitrobenzoateHCID 23291046—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product2-Nitro-4-t-butoxycarbonyl-benzoylfluorideHCID 19076184—

Reaction Steps

To a stirred solution of the above di-ester ((7), 7.28 g, 26 mmol) in dioxane (100 mL) was added aq. 1N NaOH (30 mL). The reaction was stirred for 6 h, acidified with aq. 1N HCl (30 mL), extracted with ethyl acetate, washed with brine, dried (MgSO4) and evaporated under reduced pressure to give the corresponding acid which was used as is in the next reaction. To a stirred solution of the above acid (6.68 g, 25 mMol) under Ar in dry CH2Cl2 (75 mL) was added pyridine (2.1 mL, 25 mMol) followed by cyanuric fluoride (1.56 mL, 17 mMol). After stirring for 2 h the reaction became a thick suspension. The reaction was then evaporated under reduced pressure, taken up in ether (150 mL) and filtered through a pad of celite to remove insoluble materials. The filtrate was washed with cold water, dried (MgSO4), filtered and evaporated under reduced pressure to give the crude acid fluoride (8) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05773512
Source datasetuspto-grants-1998_06
ORD IDord-c34bde1f2c9d4eeb8fb3a7a607926471
Source noteuspto-grants-1998_06