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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220160Generated: October 30, 2026

Ethylene Glycol → HCID 86591408, compound

https://huagongshe.com/reaction/2220160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantHCID 67354698HCID 67354698—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventTolueneHCID 1140—
ProductHCID 86591408HCID 8659140896%

Reaction Steps

4-[(3-oxo-1-pyrrolidinyl)sulfonyl]benzonitrile 23b (11.6 g, 46.3 mmol) was suspended in toluene (110 ml) and stirred at room temp. Ethylene glycol (6.2 ml, 6.9 g, 111 mmol) and para-toluene sulphonic acid monohydrate (100 mg, 0.53 mmol) were added. The reaction mixture was heated to reflux under Dean-Stark conditions and monitored by water collection and TLC (5% methanol in DCM). If necessary for the completion of the reaction (typically within 3h), further portions of p-TSA were added. When complete the reaction mixture was washed with saturated sodium bicarbonate solution (55 ml) and water (2×55 ml). The organic layer was filtered through cotton wool and then concentrated in vacuo to approximately 50 ml or until precipitation started. Hexane (150 ml) was added and the suspension stirred at 0-5° C. for 10-20 min, filtered and washed with hexane (2×50 ml). The residue was air dried to yield 13.0 g (96%) ketal 4-(1,4-dioxa-7-azaspiro[4.4]non-7-ylsulfonyl)benzonitrile 23c.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417058B2
Source datasetuspto-grants-2008_08
ORD IDord-f92cb459754e4bcab34cea426d2f7397
Source noteuspto-grants-2008_08