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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417761Generated: October 30, 2026

Chloroform → HCID 86638315, compound

https://huagongshe.com/reaction/417761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
Reactant1-BromohexadecaneHCID 8213—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzaldehyde, 2,4,6-trihydroxy-HCID 68099—
SolventDimethylformamideHCID 6228—
ProductHCID 86638315HCID 8663831550%

Reaction Conditions

Temperature70 °C

Reaction Steps

2,4,6-Trihydroxybenzaldehyde (435 mg, 2.53 mmol), 1-bromohexadecane (4.58 g, 15.0 mmol), K2CO3 (1.04 g, 4.52 mmol) and KI (70 mg, 0.42 mmol) were mixed in DMF (15 ml), followed by stirring at 70° C. for 20 hours. The resulting reaction product was cooled to 20° C., and chloroform (100 ml) was added thereto to separate into an organic phase and an aqueous phase. The subsequent operations are the same as in Example 1, and therefore are omitted to describe. Thus, white solid 2,4,6-trihexadecyloxybenzaldehyde (2a) was obtained (1.04 g, yield: 50%). It was confirmed by 1H NMR quantitative analysis that 2a is 2,4,6-trihexadecyloxybenzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08092773B2
Source datasetuspto-grants-2012_01
ORD IDord-af7162d0c3394b569d0c069ed31daef9
Source noteuspto-grants-2012_01