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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171687Generated: November 1, 2026

Sodium borohydride → HCID 23138766, compound

https://huagongshe.com/reaction/1171687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23139066HCID 23139066—
ProductHCID 23138766HCID 2313876668%

Reaction Steps

Following a procedure similar to that described in Example 150-(d), (E)-3-{[1-(methoxycarbonylmethyl)-1H-tetrazol-5-yl]methylidene}-1-(triphenylmethyl)piperidin-4-one (Example 150-(c), 2.2 g) was reduced with sodium borohydride. Purification gave the title compound (1.5 g, yield: 68%) as a pale yellow amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829580B2
Source datasetuspto-grants-2010_11
ORD IDord-9ed2529be2ea479bb11b94d506c217c1
Source noteuspto-grants-2010_11