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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746080Generated: October 31, 2026

Dansyl chloride → HCID 86614223, compound

https://huagongshe.com/reaction/1746080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDansyl chlorideHCID 11801—
Reactant2-Hydroxyethyl acrylateHCID 13165—
ReactantDiisopropylethylamineHCID 81531—
SolventDichloromethaneHCID 6344—
ProductHCID 86614223HCID 8661422356.5%

Reaction Steps

To a solution of 2-hydroxyethyl acrylate (25.8 mg, 0.2 mmol) in 2 ml of freshly distilled CH2Cl2 was added diisopropylethylamine (DIPEA, 0.35 ml, 0.2 mmol) dropwise at 0° C. Dansyl chloride (50.0 mg, 0.19 mmol) was then added dropwise, and the resultant mixture was stirred at room temperature until TLC indicated the disappearance of starting material. The reaction was quenched with a 5% solution of NH4Cl and extracted (3×20 ml) with CH2Cl2. The combined organic layers were dried over anhydrous MgSO4 and purified with column chromatography on silica gel (1:4, EtOAc:hexanes) to give 37.5 mg (56%) of 2-(5-dimethylamino-naphthalene-1-sulfonyloxy)-ethyl acrylate as a yellow semi solid. 1H NMR (250 MHz) δ 8.61 (d, J=8.6 Hz, 1H), 8.26 (t, J=6.3 Hz, 2H), 7.56 (m, 2H), 7.20 (d, J=7.7 Hz, 1H), 6.19 (dd, J=16.5, 2.5 Hz, 1H), 5.80 (dd, J=16.5, 10.3 Hz, 1H), 5.71 (dd, J=16.5, 10.3 Hz, 1H), 4.25 (m, 4H), 2.88 (s, 6H). 13C NMR (63 MHz) δ 158.0, 151.7, 131.8, 131.5, 130.9, 130.6, 129.8, 128.8, 127.3, 123.0, 119.4, 115.6, 67.8, 61.5, 45.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09149440B2
Source datasetuspto-grants-2015_10
ORD IDord-06120a6b1a444b4998f7573bd30c757a
Source noteuspto-grants-2015_10