HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707525Generated: October 30, 2026
Ethyl orthoformate → HCID 118162409, compound
https://huagongshe.com/reaction/707525
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | 1211531-38-2 | HCID 72212809 | — |
| Catalyst | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 118162409 | HCID 118162409 | 81.3% |
Reaction Steps
To a mixed solution of a commercially available product of 6-chloro-5-fluoropyridine-2-carbaldehyde (820 mg, 5.14 mmol) and ethanol (10.0 mL) were added triethyl orthoformate (2.56 mL, 15.4 mmol) and pyridinium p-toluenesulfonate (64.6 mg, 0.257 mmol) at room temperature. The resultant mixture was stirred at 80° C. for 5 hours. The reaction mixture was concentrated under a reduced pressure, water was added to the residue, and the resultant solution was extracted with ethyl acetate two times. An organic layer was dried over anhydrous magnesium sulfate and then filtrated. The solvent was evaporated under a reduced pressure, to give a crude product (977 mg) of the title compound. The product was used in the subsequent reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09174998B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-8d5104c210344dbcb3ee2593fc42fc4d |
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| Source note | uspto-grants-2015_11 |
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