HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527562Generated: October 30, 2026
Hexane → Ethyl (2,6-bis{[(methyloxy)methyl]oxy}phenyl)(oxo)acetate
https://huagongshe.com/reaction/527562
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexane | HCID 8058 | — |
| Reactant | Ethoxalyl chloride | HCID 20884 | — |
| Reactant | 1,3-Bis(methoxymethoxy)benzene | HCID 12222682 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl (2,6-bis{[(methyloxy)methyl]oxy}phenyl)(oxo)acetate | HCID 67235675 | 53.1% |
Reaction Steps
To a solution of 1,3-bis{[(methyloxy)methyl]oxy}benzene (Intermediate 79, 2.19 g) in dry tetrahydrofuran (10 ml) at room temperature BuLi 1.6M in hexane (8.29 ml, 13.26 mmol) was added and the reaction mixture was stirred for 30 minutes at the same temperature. The mixture was cooled to −78° C. and it was added (via cannulation) to a solution of ethyl chloro(oxo)acetate (2.263 g, 16.57 mmol) in dry tetrahydrofuran (10 ml) at −78° C. The reaction mixture was stirred at −78° C. for 30 minutes. The reaction was quenched with an aqueous saturated solution of ammonium chloride (10 ml) and extracted with ethyl acetate (2×30 ml). Combined organic layers were dried over sodium sulphate, filtered and evaporated. The residue was purified by flash chromatography (Biotage system) on silica gel using a 100 g SNAP column and cyclohexane to cyclohexane/ethyl acetate 8:2 as eluent affording the title compound as a light yellow oil (1.75 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346790B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-6d68b139a2c24b4799b8a38a9167e668 |
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| Source note | uspto-grants-2016_05 |
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