Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479385Generated: October 30, 2026

Benzyl Alcohol → HCID 18770464, compound

https://huagongshe.com/reaction/479385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 18770431HCID 18770431—
SolventTolueneHCID 1140—
ProductHCID 18770464HCID 1877046461%

Reaction Steps

Triethylamine (0.39 ml; 2.8 mmol), diphenylphosphoryl azide (0.61 ml; 2.8 mmol) and benzyl alcohol (0.39 ml; 3.8 mmol) were added to a solution in toluene (10 ml) of 2,2-bis[(1-tert-butoxycarbonyl-4-piperidinyl)methyl]acetic acid (850 mg; 1.9 mmol) synthesized by the above process, and the mixture was stirred for 12 hours in a bath controlled at 100° C. The reaction mixture was concentrated under reduced pressure, and the resultant concentrated residue was dissolved in ethyl acetate. This solution was washed successively with a saturated aqueous solution of sodium hydrogencarbonate and saturated brine, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resultant crude oil was purified by column chromatography on silica gel, thereby obtaining 639 mg (yield: 61%) of 2-benzyloxycarbonylamino-1,3-bis(1-tert-butoxycarbonyl-4-piperidinyl)propane as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06645957B2
Source datasetuspto-grants-2003_11
ORD IDord-675424697453455faa546e598843befc
Source noteuspto-grants-2003_11