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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537642Generated: October 29, 2026

Pyridine → HCID 44475518, compound

https://huagongshe.com/reaction/537642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactanto-Toluenesulfonyl chlorideHCID 8623—
ReactantO-(2-Azidoethyl)heptaethylene glycolHCID 10960238—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 44475518HCID 4447551825%

Reaction Steps

A solution of 23-azido-3,6,9,12,15,18,21-heptaoxatricosan-1-ol (800 mg, 2.02 mmol) in pyridine (4 mL) was added dropwise to the solution of toluenesulfonyl chloride (771 mg, 4.04 mmol) and 4-dimethylaminopyridine (100 mg) in pyridine (10 mL) at room temperature. The mixture was stirred for 24 hours at room temperature. The solvent was evaporated and the crude product was purified on SiO2 column using hexanes/ethylacetate gradient 0-100% followed by ethylacetate/methanol gradient 0-100%, then purified on semipreparative HPLC (System E) to yield 280 mg (25%) of 3 as a colorless oil. 1H NMR (400 MHz, CDCl3): δ 2.45 (s, 3H), 3.38 (t, J=5.02 Hz, 2H), 3.58-3.70 (m, 28H), 4.16 (t, J=5.00 Hz, 2H), 7.34 (d, J=8.4 Hz, 2H), 7.80 (d, J=8.4 Hz, 2H); 13C NMR (100.6 MHz, CDCl3): δ 21.6, 50.7, 68.7, 69.2, 70.0, 70.5-70.8, 128.0, 129.7, 133.1, 144.7; MS ESI (m/z): [M+H]+ calcd. for C23H39N3O10S 549.24. found 549.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865122B2
Source datasetuspto-grants-2014_10
ORD IDord-c7683621d5ae4f5abf0e97243081129c
Source noteuspto-grants-2014_10