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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419450Generated: November 2, 2026

Benzyl Alcohol → HCID 178511263, compound

https://huagongshe.com/reaction/1419450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 178511262HCID 178511262—
SolventTolueneHCID 1140—
ProductHCID 178511263HCID 17851126396%

Reaction Steps

50 g (0.318 moles) of trans-4-(aminomethyl)-cyclohexane carboxylic acid, 61.7 g (0.324 moles) p-toluenesulfonic acid, 250 mL (2.4 moles) benzyl alcohol and 250 mL toluene were combined and stirred. The mixture was refluxed for 24 hours and the liberated water was removed azeotropically by means of a Dean and Stark apparatus. A clear solution was obtained after 5 hours of refluxing. The solution was allowed to cool to room temp. and the product crystallized. The mixture was vacuum filtered, washed with ether and dried in a vacuum oven to give 128.12 g (96% yield.) Reference: Greenstein, Jesse P.; Winitz, Milton. Chemistry of the Amino Acids. vol. 2, (1986), 942. 1H NMR (CD3OD) δ1.05 (m, 2H), 1.43 (m, 2H), 1.59 (m, 1H), 1.85 (m, 2H), 2.03 (m, 2H), 2.33 (m, 1H), 2.35 (s, 3H), 2.75 (d, 2H), 5.09 (s, 2H), 7.23 (d, 2H), 7.32 (m, 5H), 7.69 (d, 2H). M.P. 154°-156° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05886146
Source datasetuspto-grants-1999_03
ORD IDord-f9a251f1aae544a99e2b0ae86e05bc5e
Source noteuspto-grants-1999_03