HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192361Generated: November 4, 2026
1-((2-Bromoethoxy)methyl)-4-methoxybenzene → HCID 67311654, compound
https://huagongshe.com/reaction/2192361
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-((2-Bromoethoxy)methyl)-4-methoxybenzene | HCID 11701510 | — |
| Reactant | 1-Phenyl-cycloheptanecarboxylic acid (R)-(1-aza-bicyclo[2.2.2]oct-3-yl)ester | HCID 59179619 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 67311654 | HCID 67311654 | 148.6% |
Reaction Steps
A mixture of 1-(2-bromo-ethoxymethyl)-4-methoxy-benzene (42 mg) and 1-phenyl-cycloheptanecarboxylic acid (R)-(1-aza-bicyclo[2.2.2]oct-3-yl)ester (Example 14e) (50 mg) in MeCN (1 mL) was stirred at room temperature for 16 h then heated to 80° C. under nitrogen overnight. A further 1.1 equivalents of 1-(2-bromo-ethoxymethyl)-4-methoxy -benzene were added and the mixture was heated at 80° C. for a further 48 h. The volatiles were evaporated and the crude product was purified by silica gel chromatography eluting with 0-10% of a 10% conc. NH3/MeOH solution in dichloromethane give 61 mg of an oil that was purified further by reverse phase HPLC (Gemini 5 μM C6 phenyl column) eluting with 5-95% MeOH/H2O containing 0.1% formic acid over 30 min with UV detection at 220 nm. The relevant fractions were combined and evaporated to afford the title compound (34 mg) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329729B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-00ca82777f5e4b7890fe7f4147cac5ab |
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| Source note | uspto-grants-2012_12 |
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