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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732069Generated: October 30, 2026

Formic Acid → HCID 13920729, compound

https://huagongshe.com/reaction/1732069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantWaterHCID 962—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 13749175HCID 13749175—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13920729HCID 1392072995%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of formic acid (3.05 g, 66.3 mmol) and acetic anhydride (5.4 g, 55 mmol) was heated at 60° C. for 4 hours. A solution of 6,7,8,9-tetrahydro-2-methoxy-N,10-dimethylpyrido[1,2-a]indol-9-amine (2 g, 8.2 mmol, described in Example 27) in dry tetrahydrofuran (20 mL) was added upon cooling to the resultant mixed anhydride. The reaction mixture was stirred at 25° C. overnight, poured into water (40 mL), and extracted with ether (3×40 mL). The combined extracts were washed successively with 5% hydrochloric acid (50 mL), 5% aqueous sodium bicarbonate (60 mL), and water (80 mL). The ethereal solution was dried over MgSO4, filtered, and evaporated to afford 2.1 g (95%) of the title formamide as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04624954
Source datasetuspto-grants-1986_11
ORD IDord-d772bea0456348f19b9d23138059bf58
Source noteuspto-grants-1986_11