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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417617Generated: October 29, 2026

Sodium borohydride → HCID 55036, compound

https://huagongshe.com/reaction/2417617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13298561HCID 13298561—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 55036HCID 5503699.5%

Reaction Steps

To a solution of 2-[4-[2-(3,4-dimethoxyphenyl)-2-oxoethyl]-1-piperazinyl]-2,4,6-cycloheptatrien-1-one (1.33 g, described above) in methanol (20 ml) and chloroform (5 ml), sodium borohydride (0.31 g) was added portionwise over a period of one hr. The solvent was then removed under vacuum. The residue was taken up in chloroform, washed with water, ammonium chloride solution followed by water, dried and evaporated to give the title compound (1.33 g): mp 122°-124° C.; ir(CHCl3) 3420, 1565, 1260 and 1140 cm-1 ; uv max(MeOH) 352 (ε=10040), 256 (ε=15660) and 227 nm (ε=20250); nmr(CDCl3) δ2.6 (m, 6H), 3.3 (m, 4H), 3.85 (s, 6H), 4.7 (m,1H) and 6.8 (m,6H); and Anal. Calcd for C21H26N2O4 : C, 68.08% H, 7.08% N, 7.56% and Found: C, 67.78% H, 7.06% N, 7.36%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04469695
Source datasetuspto-grants-1984_09
ORD IDord-c7fb2629372847f18e853da843972340
Source noteuspto-grants-1984_09