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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048484Generated: October 30, 2026

1,3-Benzothiazole-2-carbaldehyde → HCID 13444760, compound

https://huagongshe.com/reaction/1048484

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Benzothiazole-2-carbaldehydeHCID 241608—
ReactantHCID 178418443HCID 178418443—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13444760HCID 13444760—

Reaction Steps

To a solution of 1,3-benzothiazole-2-carbaldehyde (0.96 g, 5.88 mmol) in THF (15.0 mL) was added ethylmagnesium bromide (1.0 M solution in THF, 12.0 mL, 12.0 mmol, 2 eq), slowly over 15 minutes (an exotherm was observed). The resulting dark red solution was stirred at room temperature for 55 minutes, then quenched with saturated aqueous ammonium chloride solution (4 mL). The mixture was then concentrated under reduced pressure. Purification by flash chromatography on silica gel (0-70% EtOAc in hexanes gradient) provided the title compound as a red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569341B2
Source datasetuspto-grants-2013_10
ORD IDord-acc156a35e9342fca3149f66eb3fe25a
Source noteuspto-grants-2013_10