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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390917Generated: November 2, 2026

Dibenzylamine → HCID 12952415, compound

https://huagongshe.com/reaction/1390917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibenzylamineHCID 7656—
ReactantHCID 12952395HCID 12952395—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 12952415HCID 12952415—

Reaction Steps

A solution of dibenzylamine (3.34 g) in butanone (10 ml) was added to a vigorously sitrred suspension of 5-(2-bromoacetyl)-2-(1-piperidinyl)benzenesulphonamide, hydrobromide (2.5 g) in butanone (100 ml). After 3 hours the mixture was filtered and the filtrate concentrated to a yellow oil. This oil was dissolved in ethanol (100 ml) and treated with sodium broohydride (0.42 g) at room temperature. After 1 hour, excess borohydride was destroyed with 2N hydrochloric acid. Ethanol was removed, the residue basified with 8% sodium bicarbonate solution and extracted with ethyl acetate (3 × 100 ml). The extracts were washed with water (100 ml), dried, and concentrated to a pale yellow oil (2.7 g). This was chromatographed on Merck Kieselgel 60 (50 g) to give the product as a white solid, 2 g, m.p. 133°-142°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04140713
Source datasetuspto-grants-1979_02
ORD IDord-a9c716205fb842c08d154846be5e6f16
Source noteuspto-grants-1979_02