HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544443Generated: November 1, 2026
(2-Phenoxy-5-thiazolyl)-methanol → (2-Phenoxy-5-thiazolyl)-methanal
https://huagongshe.com/reaction/544443
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (2-Phenoxy-5-thiazolyl)-methanol | HCID 13106154 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | (2-Phenoxy-5-thiazolyl)-methanal | HCID 13106151 | 77.8% |
Reaction Steps
40 g of manganese dioxide were added to a solution of 10 g of (2-phenoxy-5-thiazolyl)-methanol in 250 ml of benzene and the mixture was stirred at 40° C. for 5 hours and was filtered. The filtrate was evaporated to dryness and the residue was chromatographed over silica gel.Elution with a 7-3 methylene chloride-ethyl acetate mixture yielded 7.7 g of (2-phenoxy-5-thiazolyl)-methanal melting at 50° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04450169 |
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| Source dataset | uspto-grants-1984_05 |
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| ORD ID | ord-443ad994da514fe5b5c8f35a5e6df95e |
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| Source note | uspto-grants-1984_05 |
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