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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735883Generated: October 30, 2026

Butyl Formate → HCID 53685709, compound

https://huagongshe.com/reaction/1735883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl FormateHCID 11614—
ReactantHCID 54324822HCID 54324822—
ProductHCID 53685709HCID 53685709—

Reaction Steps

A solution of the (S)-(5,7-difluoro-1,2,3,4-tetrahydronaphthalen-2-ylamino) acetonitrile in butyl formate (8.7 M, 240 mL, 2.10 mol) was heated to reflux and stirred under nitrogen for 19 hours. The solvents were removed under reduced pressure, toluene was added and then evaporated. Drying gave (S)-N-(cyanomethyl)-N-(5,7-difluoro-1,2,3,4-tetrahydronaphthalen-2-yl)formamide as an oily residue (53.2 g). A stirring mixture of the formamide (53.2 g) and ethyl formate (12.4M, 48.7 mL, 0.604 mol) in 0.925 L of anhydrous THF was cooled to -15° C. A solution of potassium tert-butoxide in THF (1.0 M, 302 mL, 0.302 mol) was added over 20 minutes and the mixture was stirred for 18 hours. Evaporation of the solvent gave potassium (S)-N-(1-cyano-2-oxyvinyl)-N-(5,7-difluoro-1,2,3,4-tetrahydronaphthalen-2-yl)formamide as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05538988
Source datasetuspto-grants-1996_07
ORD IDord-8b811a70b38c43f7a2bc866c7eaf6e71
Source noteuspto-grants-1996_07