HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652006Generated: October 29, 2026
Trimethyl orthoformate → 2-(2-Bromophenyl)acetaldehyde dimethylacetal
https://huagongshe.com/reaction/652006
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 2-(2-Bromophenyl)acetaldehyde | HCID 11424180 | — |
| Reactant | NaOH brine | HCID 131715167 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(2-Bromophenyl)acetaldehyde dimethylacetal | HCID 11032130 | — |
Reaction Steps
To a solution of 10.0 grams (0.05 mole) of 2-(2-bromophenyl)acetaldehyde (from the above preparation and another similar preparation) in 50 milliliters of dry methanol, was added 50 milliliters of trimethyl orthoformate and 0.25 gram of p-toluenesulfonic acid monohydrate and the resulting mixture was heated at reflux temperature for 3.5 hours. At the end of this period, the reaction mixture was cooled and 100 milliliters of diethyl ether and 50 milliliters of a 1:1 solution of 50 percent aqueous sodium hydroxide/brine were added. The ether solution was mechanically separated, washed, dried and stripped on the rotary evaporator to obtain 2-(2-bromophenyl)acetaldehyde dimethylacetal intermediate as a yellow oil. The latter was distilled to obtain 10.5 grams (85 percent yield) of purified product as a clear oil, b.p. 65°-67° /0.2 mm.
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-d30b109b23a7433daa00e212c9d04755 |
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| Source note | uspto-grants-1987_06 |
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