Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763651Generated: November 2, 2026

Formaldehyde → HCID 20310623, compound

https://huagongshe.com/reaction/1763651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantAcetonitrileHCID 6342—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 20310593HCID 20310593—
SolventAcetic AcidHCID 176—
ProductHCID 20310623HCID 20310623—

Reaction Steps

To a solution of 9-amino-11H-pyrrolo[2,1-b][3]benzazepin-11-one (2.1 g., 10 mmoles) and 4 ml. (50 mmole) of 37% aqueous formaldehyde in 15 ml. of acetonitrile is added 1 g. (16 mmoles) of sodium cyano borohydride. A vigorous and exothermic reaction takes place and a dark residue separates. The mixture is stirred for 15 mins. and then glacial acetic acid is added dropwise until the solution tests neutral on wet pH paper. Stirring is maintained for an additional 2 hrs. The volatiles are removed under vacuum, and the residue is dissolved in chloroform. The solution is washed with base and with water, dried over sodium sulfate, and concentrated to leave a residue that is purified by chromatography on silica gel. Elution with chloroform yields 9-dimethylamino-11H-pyrrolo[2,1-b][3]benzazepin-11-one as a dark brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04112112
Source datasetuspto-grants-1978_09
ORD IDord-51fa0aaa651e4d64a7e5dcc18a8a5240
Source noteuspto-grants-1978_09