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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064385Generated: October 31, 2026

Sodium borohydride → HCID 23403780, compound

https://huagongshe.com/reaction/1064385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEther hydrochlorideHCID 10953452—
ReactantHCID 22273798HCID 22273798—
SolventMethanolHCID 887—
SolventEthyl ether methylene chlorideHCID 21881112—
ProductHCID 23403780HCID 23403780—

Reaction Steps

0.7 g (2.1 mmol) of (±)-7-[(4-phenylpiperidin-1-yl)methyl]-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-one were dissolved in 40 mL of MeOH and 0.35 g of NaBH4 were added portionwise. The reaction mixture was stirred 2 h at room temperature, the MeOH removed in vacuo, then the residue was taken up in 1N NaOH and extracted with CH2Cl2. The organic phase was dried and the solvent was removed in vacuo. The crude product was purified by chromatography, eluting with CH2Cl2 and then with a mixture CH2Cl2/MeOH 100:3 respectively, yielding 100 mg of trans isomer which was dissolved in a mixture CH2Cl2/Et2O: The solution was brought to acidic pH with Et2O/HCl and the solvent was removed in vacuo. The resulting solid was triturated with hot acetone, filtered and dried, yielding 90 mg of the title compound. m.p.>250° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969724B2
Source datasetuspto-grants-2005_11
ORD IDord-ee4e62ed18f648ee8c1987fa0bbba336
Source noteuspto-grants-2005_11