Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490123Generated: October 30, 2026

Benzyl Alcohol → HCID 178511263, compound

https://huagongshe.com/reaction/1490123

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-Stark apparatus. A clear solution was obtained after 5 hours of refluxing. The solution was allowed to cool to room temperature. 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) δ 1.05 (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 numberUS05681844
Source datasetuspto-grants-1997_10
ORD IDord-df8c00795fb9413bb6eb830d6b2f38c3
Source noteuspto-grants-1997_10