HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559483Generated: October 31, 2026
o-Fluorobenzaldehyde → HCID 57456783, compound
https://huagongshe.com/reaction/559483
Participants
| Role | Name | HCID | Charge |
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| Reactant | o-Fluorobenzaldehyde | HCID 67970 | — |
| Reactant | 2,2-Diethoxyethylamine | HCID 69524 | — |
| Product | HCID 57456783 | HCID 57456783 | — |
Reaction Steps
2-Fluorobenzaldehyde (7.45 g), was added to aminoacetaldehyde diethylacetal (9.16 g) and the reaction heated to 100° C. for 3 h. After cooling, the mixture was transferred to a separating funnel and partitioned between diethyl ether and water. The ether layer was separated, dried over magnesium sulfate, filtered and concentrated under reduced pressure to leave an oil. Distillation at 0.6-0.8 mm collecting the fraction boiling at 102-106° C. afforded the title compound as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063078B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-67f9c881a32d49b88fc7ab753872f04d |
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| Source note | uspto-grants-2011_11 |
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