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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055502Generated: November 1, 2026

1,2-Dichlorobenzene → HCID 117985969, compound

https://huagongshe.com/reaction/1055502

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichlorobenzeneHCID 7239—
ReactantHCID 118377829HCID 118377829—
CatalystPalladiumHCID 23938—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 117985969HCID 11798596951.1%

Reaction Steps

To a solution of 1-[(1R,2S,3S,4R,5S)-2,3,4-tribenzyloxy-5-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-6,8-dioxabicyclo[3.2.1]octan-1-yl]ethanol 1m (1.71 g, 2.36 mmol) in a methanol/tetrahydrofuran mixture (v/v=4/1, 30 mL) were added o-dichlorobenzene (1.74 g, 11.8 mmol) and 10% Pd/C (250 mg, 0.236 mmol) at room temperature. The mixture was stirred under H2 at room temperature for 1.5 hours and filtered. The filtrate was concentrated in vacuo. The residue was purified by preparative HPLC (prep-HPLC) to give the title compound 1 as a white solid (544 mg, 51.3%, HPLC: 99.6%). The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 451.2 [M+H]+; and 1H NMR (400 MHz, CDCl3) δ (ppm): 7.35 (m, 1H), 7.29-7.21 (m, 2H), 7.04 (m, 2H), 6.75 (m, 2H), 4.71 (br, 1H), 4.51 (br, 1H), 4.14 (m, 1H), 4.01 (m, 3H), 3.98 (m, 2H), 3.89 (m, 1H), 3.77 (m, 2H), 3.60 (m, 1H), 3.52 (br, 1H), 3.06 (br, 1H), 1.34 (t, 3H), 0.91 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394329B2
Source datasetuspto-grants-2016_07
ORD IDord-53a00ada24be4f6e94d6777b4e9d9172
Source noteuspto-grants-2016_07