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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444702Generated: October 30, 2026

Formic Acid → HCID 86602829, compound

https://huagongshe.com/reaction/1444702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantAcetic-formic anhydrideHCID 75269—
Reactant1-Aminotetralin, (R)-HCID 7058072—
SolventDiethyl EtherHCID 3283—
ProductHCID 86602829HCID 86602829—

Reaction Steps

To a solution of acetic formic anhydride (0.056 mol) (prepared by stirring acetyl anhydride (7.36 ml, 78.0 mmol) and formic acid (2.94 ml, 78.0 mmol) at 50-60° C. for 2 h then cooling to room temperature) was added (r)-1,2,3,4-tetrahydro-1-naphthylamine (8.20 g, 55.7 mmol) dropwise with stirring at such a rate that the temperature never rose above 40° C. After stirring for 30 min, 300 mL of ether was added, and the solution was stirred at room temperature overnight. The reaction was diluted with ether, washed twice with water, twice with Sat. NaHCO3, with 5% HCl, and finally with water. The organic layer was dried with Na2SO4, filtered, and evaporated to dryness. flash chomatograph (SiO2, hexane/EtOAc=1:1 to pure EtOAc) afforded (R)—N-(1,2,3,4-tetrahydronaphthalen-1-yl)formamide as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662811B2
Source datasetuspto-grants-2010_02
ORD IDord-f9bd5271e6974f409b833e757e53fb5b
Source noteuspto-grants-2010_02