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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755488Generated: November 1, 2026

2-Bromopropanedial → HCID 86700131, compound

https://huagongshe.com/reaction/1755488

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropanedialHCID 74945—
ReactantHCID 86700132HCID 86700132—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86700131HCID 8670013139%

Reaction Steps

To a solution of material from Example 112 (3.21 g, 12.19 mmol) in a mixture of THF (107 mL) and acetic acid (29 mL) is added 2-bromomalonaldehyde (3.29 g, 21.79 mmol). The resulting solution is stirred at room temp for 60 h. The reaction is diluted with water (71 mL) and the resulting slurry is stirred at room temp for 1.5 h. The slurry is extracted with EtOAc (3×300 mL), the organic layers combined, washed with brine (1×50 mL), dried over Na2SO4, filtered and evaporated to dryness. The resulting residue is purified by BIOTAGE® Silica gel chromatography on a 80 g Thompson Single Step silica cartridge using a linear gradient from 100% CHCl3 to 25% MeOH/CHCl3 over 9 column volumes to give 1.5 g (39%) of the title compound as an orange/yellow film, 1H NMR (500 MHz, methanol-d4) δ 9.65 (s, 1H), 7.97 (s, 1H), 4.49-4.37 (m, 1H), 3.93 (dd, J=13.9, 4.4 Hz, 1H), 3.72 (dd, J=14.0, 7.7 Hz, 1H), 1.45 (s, 914). LC/MS (Condition A): ret. T=2.46 min, (M+Na) 338.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169295B2
Source datasetuspto-grants-2015_10
ORD IDord-fd0630a7009944e38eda754b6674c7fe
Source noteuspto-grants-2015_10