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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719186Generated: November 2, 2026

Benzyl Alcohol → HCID 86740277, compound

https://huagongshe.com/reaction/1719186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantWaterHCID 962—
ReactantL-LysineHCID 5962—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventTolueneHCID 1140—
ProductHCID 86740277HCID 8674027762%

Reaction Steps

Nα-Banzyloxycarbonyl (L) lysine (10 g; 35.7 mmol) in benzyl alcohol (30 cm3), toluene (30 cm3) and para toluene sulphonic acid (6.93 g) was heated under reflux. The water evolved from the reaction and from the p-toluene sulphonic acid monohydrate was collected azeotropically using a Dean and Stark apparatus. Refluxing was continued until the water was no longer collected. The reaction mixture was allowed to cool, when crystals formed. The crystals were filtered off and dried, yield=5 g. The proton magnetic resonance and infrared spectra showed this compound to be the p-toluene sulphonic acid salt of the starting material. The filtrate was poured into ether (300 cm3) forming an oil. The ether was decanted off and the oil washed with ether and dried under reduced pressure. The resultant oil slowly crystallised to afford 12 g (62%) of the title compound, ν (Nujol) 3370, 1735, 1692, 1040, 1015, 820, 745, 735, 700, 685 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04539202
Source datasetuspto-grants-1985_09
ORD IDord-68f35de143194a9eab7a95d281e9f192
Source noteuspto-grants-1985_09