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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339589Generated: October 30, 2026

Salicylaldehyde → HCID 136060540, compound

https://huagongshe.com/reaction/339589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylaldehydeHCID 6998—
ReactantHCID 13599214HCID 13599214—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 136060540HCID 13606054060%

Reaction Steps

Prepared as described in the Alkene Formation section using diethyl 4-(6-methylbenzothiazol-2-yl)benzylphosphonate (0.30 g, 0.80 mmol) in dry THF (25 ml), potassium t-butoxide (0.19 g, 1.68 mmol) and 2-hydroxybenzaldehyde (0.097 g, 0.80 mmol) in dry THF (10 ml) to give the title compound (0.16 g, 60%) as a yellow solid after work-up and flash chromatography (1:1 Hexane/EtOAc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895313B2
Source datasetuspto-grants-2014_11
ORD IDord-be5a38215d5c44bf87ac71c782072809
Source noteuspto-grants-2014_11