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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182718Generated: November 3, 2026

Formaldehyde → HCID 68629339, compound

https://huagongshe.com/reaction/1182718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 67363168HCID 67363168—
SolventMethanolHCID 887—
ProductHCID 68629339HCID 6862933930.4%

Reaction Steps

A mixture of 1-bromo-8-chloro-5,6-dihydro-4H-2,3,5,10b-tetraaza-benzo[e]azulene (1.9 g, 6.4 mmol) and paraformaldehyde (1.5 g, 51 mmol) in methanol (64 ml) was heated at reflux for 16 h. After cooling to 0° C. sodium cyanoborohydride (0.8 g, 13 mmol) was added. The reaction mixture was allowed to warm to room temperature and stirred for 3 h. After quenching with 1 M aqueous sodium hydroxide solution (200 ml) the aqueous layer was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo. Flash chromatography over aminopropyl-modified silica gel with n-heptane/ethyl acetate as eluent gave the title compound (0.61 g) as white solid with a purity of ca. 85% as assessed by 1H-NMR. MS m/e: 313 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664216B2
Source datasetuspto-grants-2014_03
ORD IDord-f7bd9bd0a989408992d8c0ec69ad584e
Source noteuspto-grants-2014_03