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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296283Generated: October 30, 2026

Sodium borohydride → HCID 13228378, compound

https://huagongshe.com/reaction/2296283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13228374HCID 13228374—
SolventMethanolHCID 887—
ProductHCID 13228378HCID 13228378—

Reaction Steps

Portionwise 0.2 g (52 mmol) of sodium borohydride was added to a solution of 3.0 g (6.3 mmol) of 8-chloro-6-(2-chlorophenyl)-2,5-dimethyl-2H,4H-pyrrolo[3,4-d][2]benzazepin-5-ium iodide in 50 ml of methanol which was cooled to 0°. The mixture was stirred at 0° for 20 min followed by the removal of the methanol at reduced pressure. The residue was partitioned between methylene chloride and water. The methylene chloride solution was washed with water and saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, and concentrated at reduced pressure to give a pale yellow oil. Crystallization from ether gave colorless crystals, mp 154°-155°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04428878
Source datasetuspto-grants-1984_01
ORD IDord-7c607dc90b1c4f2a96720de0914eb489
Source noteuspto-grants-1984_01