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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437452Generated: November 2, 2026

Dichloromethane → HCID 57941180, compound

https://huagongshe.com/reaction/1437452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 57941176HCID 57941176—
SolventWaterHCID 962—
ProductHCID 57941180HCID 57941180—

Reaction Steps

To a stir bar equipped flask containing 4-(2,5-difluorophenyl)-6-(3-methoxyphenyl)-1,2,3,6-tetrahydropyridne (1-5, 0.6 g, 0.19 mmol) was added dichloromethane (15 mL) followed successively by TEA (0.14 mL, 0.19 mmol), and acetic anhydride (0.06 mL, 0.59 mmol). The resulting solution stirred for 10 min. Water was added (2 mL), and then the reaction was washed with dichloromethane (2×30 mL). The organics were dried over sodium sulfate, filtered, and concentrated under reduced pressure. The crude reside was purified by reverse phase liquid chromatography (0.1% TFA) to give 1-acetyl-4-(2,5-difluorophenyl)-6-(3-methoxyphenyl)-1,2,3,6-tetrahydropyridine (1-6). 1H NMR (300 MHz, CDCl3) δ 7.26 (m, 1H), 6.96 (m, 4H), 6.82 (m, 1H); 6.36 (m, 1H), 6.20 (m, 1H), 3.82 (s, 3H), 3.80 (m, 2H); 3.40 (dt, J=11.9, 4.2 Hz, 1H); 2.74 (m, 1H); 2.42 (dd, J=16.0, 1.0 Hz, 1H), 2.20 (s, 3H); MS 344.1 found, 343.3 (M+H+) required.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622489B2
Source datasetuspto-grants-2009_11
ORD IDord-5762a4490344461ca20e96ce0cb582ed
Source noteuspto-grants-2009_11