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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176962Generated: November 2, 2026

Dichloromethane → HCID 68775436, compound

https://huagongshe.com/reaction/1176962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 86620323HCID 86620323—
SolventAcetoneHCID 180—
SolventPropan-2-one--water (1/1)HCID 18366337—
ProductHCID 68775436HCID 68775436—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of [2-(3,4-bis-dodecyloxy-phenyl)-[1,3]dithian-2-yl]-(4-bromo-phenyl)-methanol (JYC-I-049-A). (10.99 g, 0.015 mol) in 400 mL of acetone was added dropwise to a solution of N-bromosuccinimide (NBS) (45.4 g, 0.255 mol) in 300 mL of 3% water/acetone (v/v) at 0° C. in an ice bath. The reaction mixture was stirred at 0° C. and gradually warmed up to room temperature over 30 min. The mixture was then poured into a saturated aqueous NaSO3 solution (400 mL) and dichloromethane (400 mL). The mixture was stirred for an additional 10 min. The organic layer was washed with water several times and dried over anhydrous MgSO4. The solvent was removed under reduced pressure to give a pale yellow solid. Purification was carried out by first recrystallization from hexanes, followed by column chromatography (silica gel, hexanes:dichloromethane=1:1 (v/v)) to afford two products. The major product, 1-(3,4-bis-dodecyloxy-phenyl)-2-(4-bromo-phenyl)-ethane-1,2-dione (JYC-I-053-B), was isolated as a yellow solid. (3.21 g, 33%). 1H NMR (200 MHz, CDCl3, δ): 7.81 (d, J=8.7 Hz, 2H), 7.62 (d, J=8.7 Hz, 2H), 7.54 (d, J=2.0 Hz, 1H), 7.39 (dd, J=2.0 Hz, 8.4 Hz, 1H), 6.83 (d, J=8.4 Hz, 1H), 4.04 (t, J=6.6 Hz, 2H), 4.03 (t, J=6.6 Hz, 2H), 1.82 (m, 4H), 1.20-1.52 (m, 40H), 0.85 (t, J=6.2 Hz, 6H). 13C{(H} NMR (50 MHz, CDCl3, δ): 193.60, 192.64, 155.37, 149.46, 132.30, 132.08, 131.24, 130.17, 126.22, 125.60, 112.13, 111.58, 69.23, 69.15, 31.91, 29.61, 29.36, 29.03, 28.88, 25.97, 25.90, 22.68, 14.10. HRMS-FAB (m/z): [M+H]+ calcd for C38H58BrO4, 657.3518; found, 657.3515. Anal. Calcd for C39H57BrO4: C, 69.39; H, 8.73. Found: C, 69.27; H, 8.71. The minor product, 1-(2-bromo-4,5-bis-dodecyloxy-phenyl)-2-(4-bromo-phenyl)-ethane-1,2-dione (JYC-I-053-A), was isolated as a white solid (0.31 g). 1H NMR (200 MHz, CDCl3, δ): 7.85 (d, J=8.6 Hz, 2H), 7.65 (d, J=8.6 Hz, 2H), 7.39 (s, 1H), 6.98 (s, 1H), 4.02 (t, J=6.6 Hz, 2H), 4.01 (t, J=6.6 Hz, 2H), 1.82 (m, 4H), 1.20-1.52 (m, 36H), 0.86 (t, J=6.4 Hz, 6H). HRMS-FAB (m/z): [M+H]+ calcd for C38H57Br2O4, 735.2624; found, 735.2638.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842830B2
Source datasetuspto-grants-2010_11
ORD IDord-bc7d24ad755c4c07a9eced06fbb50a37
Source noteuspto-grants-2010_11