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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616910Generated: October 27, 2026

Formaldehyde → 7-Iodo-1,2,3,4-tetrahydro[1]benzofuro[2,3-c]pyridine

https://huagongshe.com/reaction/1616910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant2-(6-Iodobenzofuran-3-yl)ethanamine hydrochlorideHCID 67324003—
CatalystFormaldehydeHCID 712—
SolventHydrochloric AcidHCID 313—
Product7-Iodo-1,2,3,4-tetrahydro[1]benzofuro[2,3-c]pyridineHCID 67324876103.8%

Reaction Conditions

Temperature70 °C

Reaction Steps

Paraformaldehyde (8.9 g, 0.297 mol) was added to a solution of 2-(6-iodo-1-benzofuran-3-yl)ethanamine hydrochloride (80 g; 0.247 mol) in 1N HCl (500 mL) under N2. After 2 h stirring at 70° C., another portion of paraformaldehyde (740 mg) was added. The reaction mixture was cooled down to r.t., filtered, the resulting solid was washed with 1N HCl (100 mL), dried overnight under house vacuum to afford 76.7 g of the title product as a hydrochloric acid salt. 1H-NMR (400 MHz, CDCl3): δ 2.06 (bt, 2H), 2.92 (bt, 2H), 4.37 (s, 2H), 7.45 (d, 1H) 7.62 (dd, 1H), 8.05 (d, 1H), 10.04 (bs, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765779B2
Source datasetuspto-grants-2014_07
ORD IDord-aa96e2549f954b9093dec4d12cfdf7d5
Source noteuspto-grants-2014_07