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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763635Generated: October 31, 2026

Formaldehyde → HCID 20310637, compound

https://huagongshe.com/reaction/1763635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 13152894HCID 13152894—
SolventAcetic AcidHCID 176—
ProductHCID 20310637HCID 20310637—

Reaction Steps

To a solution of 9-amino-6,11-dihydro-5H-pyrrolo[2,1-b][3]benzazepin-11-one (2.1 g., 10 mmoles) and 4 ml. (50 mmoles) of 37% aqueous formaldehyde in 15 ml. of acetonitrite 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 minutes and then glacial acetic acid is added dropwise until the solution tests neutral on wet pH paper. Stirring is maintained for an additional 2 hours. 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-6,11-dihydro-5H-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-d9438a24478f4663b9011c832e326347
Source noteuspto-grants-1978_09