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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111966Generated: October 30, 2026

Sodium borohydride → HCID 13355660, compound

https://huagongshe.com/reaction/1111966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13355652HCID 13355652—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13355660HCID 13355660—

Reaction Steps

3 gm of sodium borohydride were added at room temperature to a solution of 7.5 gm of 4'-amino-3'-bromo-5'-cyano-2-cyclopropylamino-acetophenone in 200 ml of tetrahydro-furan and 100 ml of water, and the mixture was stirred for one hour. Thereafter, the excess sodium borohydride was destroyed by addition of acetone. The insoluble part of the mixture was filtered off, and the solvents were distilled out of the filtrate in vacuo. The residue was dissolved in hot isopropanol, and the hydrochloride of 1-(4'-amino-3'-bromo-5'-cyano-phenyl)-2-cyclopropylanino-ethanol was precipitated by addition of isopropanolic hydrochloric acid, and recrystallized from isopropanol. M.p. 190°-193° C. (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04119710
Source datasetuspto-grants-1978_10
ORD IDord-94fbaf1d7ef84cdeb3fded3c5a8d5493
Source noteuspto-grants-1978_10