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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366762Generated: November 1, 2026

Formaldehyde → HCID 178484113, compound

https://huagongshe.com/reaction/1366762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 178484836HCID 178484836—
CatalystAcetic AcidHCID 176—
SolventAcetonitrileHCID 6342—
ProductHCID 178484113HCID 178484113—

Reaction Steps

A couple of drops of glacial acetic acid were added to a solution of trans-6(4-methylaminocyclohexyloxy)-2H-isoquinolin-1-one (Example 12; 25 mg, 92 μmol) and formaldehyde (40 μL) in acetonitrile (1 ml). The mixture was stirred for 20 minutes and then sodium triacetoxyborohydride (100 mg) was added. The mixture was stirred at ambient temperature for 16 hours then concentrated in vacuo. The residue was partitioned between chloroform/isopropanol (3:1) and aqueous sodium hydrogen carbonate. The organic layer was separated then concentrated to give a residue that was purified by prep-HPLC to give trans-6(4-dimethylaminocyclohexyloxy)-2H-isoquinolin-1-one, EI-MS: m/z=287.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893088B2
Source datasetuspto-grants-2011_02
ORD IDord-74800ce085384da9b50111bffef7a9f1
Source noteuspto-grants-2011_02