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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815938Generated: November 1, 2026

Acetyl chloride → Acetic acid 7-allyl-1H-indazol-6-yl ester

https://huagongshe.com/reaction/1815938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant7-Allyl-1H-indazol-6-olHCID 135843647—
SolventTetrahydrofuranHCID 8028—
ProductAcetic acid 7-allyl-1H-indazol-6-yl esterHCID 69566045—

Reaction Steps

A solution of the product from Step B (6.35 g, 37 mmol) in THF (100 mL) containing triethylamine (7.6 ml, 55 mmol) was stirred for 5 minutes at ambient temperature, cooled to 0° C. (ice bath), and acetyl chloride (2.63 mL, 37 mmol) was added. The mixture was stirred at 0° C. for 2 hours, additional acetyl chloride (0.26 mL, 3.7 mmol) was added, and the mixture stirred for 10 min at which point another portion of acetyl chloride (0.26 ml, 3.7 mmol) was added and stirring continued for 15 min. The reaction was quenched with triethyl amine (1 mL) and saturated aqueous sodium bicarbonate (100 mL) and extracted with ethyl acetate (100 mL). The extract was dried (MgSO4) and evaporated to an oil (9.27 g) which was purified by chromatography (silica, 10% to 50% EtOAc/hexane) to give a white solid, (3.50 g, 44%): LC/MS (+APCI) m/z 217 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881749B2
Source datasetuspto-grants-2005_04
ORD IDord-040a4425ba55440091d6a07ecc85b2fc
Source noteuspto-grants-2005_04