Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171733Generated: November 2, 2026

Dichloromethane → HCID 23138794, compound

https://huagongshe.com/reaction/1171733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23138831HCID 23138831—
SolventEthanolHCID 702—
ProductHCID 23138794HCID 2313879437%

Reaction Steps

(E)-3-({2-[3-(Ethoxycarbonyl)propyl]-2H-tetrazol-5-yl}methylidene)-1-(triphenylmethyl)piperidin-4-one (3.93 g) was reduced with sodium borohydride (281 mg) in a mixed solvent of dichloromethane (30 ml) and ethanol (30 ml) in a similar manner to that mentioned in Example 138 (c), and the crude product obtained by conventional extraction procedures was purified by chromatography on silica gel using a mixture of ethyl acetate and hexane (1:9 to 7:3) as the eluent to afford the title compound as a yellow oil (1.46 g, yield: 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829580B2
Source datasetuspto-grants-2010_11
ORD IDord-5c59255ba917438a828f7e09d6cae192
Source noteuspto-grants-2010_11