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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoformateHCID 9005—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant2-(2-Bromophenyl)acetaldehydeHCID 11424180—
ReactantNaOH brineHCID 131715167—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
Product2-(2-Bromophenyl)acetaldehyde dimethylacetalHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04670443
Source datasetuspto-grants-1987_06
ORD IDord-d30b109b23a7433daa00e212c9d04755
Source noteuspto-grants-1987_06