HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652005Generated: October 28, 2026
Diethyl Ether → 2-(2-Bromophenyl)acetaldehyde
https://huagongshe.com/reaction/652005
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-(2-Bromophenyl)ethan-1-ol | HCID 2734089 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(2-Bromophenyl)acetaldehyde | HCID 11424180 | — |
Reaction Steps
A solution of 9.11 grams (0.045 mole) of 2-(2-bromophenyl)ethanol in 35 milliliters of methylene chloride was added to a stirred suspension of 14.62 grams (0.063 mole) of pyridinium chlorochromate in 75 milliliters of methylene chloride at ambient temperature whereupon a slightly exothermic reaction took place with the formation of a black reaction mixture. Stirring was continued for 15 hours at ambient temperature; then 150 milliliters of ether was added and the mixture filtered through silica gel on a pad of celite. The insoluble residue was washed with 100 milliliters of ether, filtered, the ether solutions combined and the solvents evaporated on a rotary evaporator to recover as residue, 8.0 grams (90 percent) of the desired 2-(2-bromophenyl)acetaldehyde intermediate as an oil. The oil had an Rf of 0.6 on silica gel when eluted with one percent methanol in chloroform.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04670443 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-b2525f8437c94b5b999783693b4d4a5f |
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| Source note | uspto-grants-1987_06 |
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