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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106039Generated: October 29, 2026

Ethylene Glycol → HCID 12811387, compound

https://huagongshe.com/reaction/1106039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantBenzeneHCID 241—
ReactantN-Carbobenzyloxy-4-keto-L-prolineHCID 11076282—
SolventWaterHCID 962—
ProductHCID 12811387HCID 1281138797%

Reaction Steps

A stirred mixture of 12.8 g (0.049 mole) of N-carbobenzyloxy-4-keto-L-proline, 53 ml (0.095 mole) of ethylene glycol, and 0.35 g of p-toluenesulfonic acid H2O in 1.31 l. of benzene is heated and the resulting solution is refluxed for 7 hours (water formed is collected in a Dean-Stark apparatus). After standing overnight at room temperature, the lower glycol layer is separated and the benzene solution is washed with 150 ml of saturated sodium chloride, dried (MgSO4), and the solvent evaporated to give 14.6 g of N-carbobenzyloxy-4,4-ethylenedioxy-L-proline as a syrupy residue. The latter is dissolved in 60 ml of ethanol, filtered, treated with 5 g of cyclohexylamine, and diluted with ether. On seeding and rubbing, the crystalline cyclohexylamine salt separates; weight after cooling overnight, 9.0 g., m.p. 179°-180° (s. 173°). The material is recrystallized from acetonitrile, m.p. 182°-184° (s. 179°), [α]D26 -21° (c, 1 % in EtOh).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04311705
Source datasetuspto-grants-1982_01
ORD IDord-51ca561d4aee4e48a126e292418e7204
Source noteuspto-grants-1982_01