HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055529Generated: November 1, 2026
1,2-Dichlorobenzene → HCID 117986011, compound
https://huagongshe.com/reaction/1055529
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichlorobenzene | HCID 7239 | — |
| Reactant | HCID 118377815 | HCID 118377815 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | HCID 117986011 | HCID 117986011 | 77.6% |
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]ethyl 2,2-dimethyl propanoate 14a (120 mg, 0.15 mmol) in a methanol/tetrahydrofuran mixture (v/v=4/1, 10 mL) were added o-dichlorobenzene (0.08 mL, 0.72 mmol) and 10% Pd/C (19 mg, 0.02 mmol) in turn at room temperature. The mixture was stirred at room temperature under H2 for 4 hours and filtered. The filtrate was concentrated in vacuo. The residue was purified by silica gel chromatography eluted with PE/EtOAc(v/v)=4/1 to give the title compound 14 as a white solid (62.3 mg, 77.6%, HPLC: 85.3%). The compound was characterized by the following spectroscopic data: MS(ESI, pos. ion) m/z: 580.3[M+HCOO]−; and 1H NMR (600 MHz, DMSO-d6) δ(ppm): 7.42 (m, 2H), 7.32 (m, 1H), 7.08 (m, 2H), 6.82 (m, 2H), 5.38 (brs, 1H), 5.06 (m, 1H), 4.04 (d, 1H), 3.97 (m, 3H), 3.57 (d, 1H), 3.52 (d, 1H), 3.47 (m, 3H), 1.30 (t, 3H), 1.23 (d, 3H), 1.10 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394329B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-3d9acb7c5c8c47c189cb0500b1513be3 |
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| Source note | uspto-grants-2016_07 |
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