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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980327Generated: October 30, 2026

p-Toluenesulfonic acid → HCID 86741215, compound

https://huagongshe.com/reaction/980327

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactantcis-1,3-dibenzyl-4-hydroxy-4-(4-(2,4,10-trioxaadamantyl)-butyl)-hexahydro-1H-thieno[3,4-d]imidazol-2-oneHCID 86741216—
SolventTolueneHCID 1140—
ProductHCID 86741215HCID 8674121596.3%

Reaction Steps

910 mg (1.68 mmol) of cis-1,3-dibenzyl-4-hydroxy-4-(4-(2,4,10-trioxaadamantyl)-butyl)-hexahydro-1H-thieno[3,4-d]imidazol-2-one (prepared in accordance with Example 1) are dissolved in 50 ml of toluene and the solution is treated with 20 mg of p-toluenesulphonic acid. The solution is heated to boiling and 20 ml of toluene are distilled off within 1 hour. Thereafter, the solution is evaporated to dryness. The residue remaining is chromatographed on silica gel. Elution with toluene, toluene/ethyl acetate (9:1) and (8:2) gives 839 mg (96% of theory) of cis-1,3-dibenzyl-4-(4-(2,4,10-trioxaadamantyl)-butylidene)-hexahydro-1H-thieno[3,4-d]imidazol-2-one in the form of a light brown oil which solidifies upon drying.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04636566
Source datasetuspto-grants-1987_01
ORD IDord-e862776c373d44d8a7091c75b1a18282
Source noteuspto-grants-1987_01