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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602178Generated: October 27, 2026

1-Boc-3-hydroxypiperidine → 1-(tert-Butoxycarbonyl)-3-[(4'-chlorobiphenyl-4-yl)methoxy]piperidine

https://huagongshe.com/reaction/602178

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Boc-3-hydroxypiperidineHCID 545699—
Reactant4'-Chloro-4-chloromethylbiphenylHCID 12773846—
Product1-(tert-Butoxycarbonyl)-3-[(4'-chlorobiphenyl-4-yl)methoxy]piperidineHCID 5899268084%

Reaction Steps

Using 1-(tert-butoxycarbonyl)-3-hydroxypiperidine (403 mg, 2.00 mmol) and 4′-chloro-4-chloromethylbiphenyl (474 mg, 2.00 mmol), the same procedure was followed as in Step 6a of Example 6 to give 672 mg (84%) of the desired compound as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902367B2
Source datasetuspto-grants-2011_03
ORD IDord-aac6f53a90d446a4aadf87b1adb8ad31
Source noteuspto-grants-2011_03