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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073122Generated: November 1, 2026

Formic Acid → HCID 14181210, compound

https://huagongshe.com/reaction/1073122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 14181206HCID 14181206—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 14181210HCID 14181210—

Reaction Steps

2.04 ml (21.5 mmol) of acetic anhydride and 0.86 ml (22.8 mmol) of formic acid were stirred for 2 h at +60° C. under nitrogen. After cooling to room temperature, 2.6 g (10 mmol) of 2-dipropylamino-8-aminomethyl-1,2,3,4-tetrahydronaphthalene were added dropwise at a maximum of +25° C. After 15 minutes post-reaction, 5 ml of ether were added. The batch was subsequently stirred for a further 18 h at room temperature and then diluted with 20 ml of ether and 20 ml of water. The aqueous phase was adjusted to pH 9 using 1 N sodium hydroxide solution and extracted with ether. The organic phase now obtained was washed with water and dried over sodium sulphate, and the solvent was removed by distillation. The residue was recrystallized from petroleum ether 60-80.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968679
Source datasetuspto-grants-1990_11
ORD IDord-22303e17fe2d4b72a9fb45197e55ef17
Source noteuspto-grants-1990_11