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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1590736Generated: October 31, 2026

3,3-Dimethylbutanoyl chloride → Methyl 3-[3-(3,3-dimethyl-1-oxo-1-butyl)-5-(quinolin-2-ylmethoxy)indol-2-yl]-2,2-dimethyl-propanoate

https://huagongshe.com/reaction/1590736

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3-Dimethylbutanoyl chlorideHCID 81514—
Reactant2,3-DihydroxybutanedioateHCID 3806114—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantMethyl 3-[5-(quinolin-2-ylmethoxy)indol-2-yl]-2,2-dimethylpropanoateHCID 18947552—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-[3-(3,3-dimethyl-1-oxo-1-butyl)-5-(quinolin-2-ylmethoxy)indol-2-yl]-2,2-dimethyl-propanoateHCID 18947551—

Reaction Steps

To a suspension of AlCl3 (5.7 g, 42 mmol) in CH2Cl2 (30 mL) at 0° C. was added 3,3-dimethylbutanoyl chloride (2.4 mL. 17 mmol). After 15 minutes at 0° C., a solution of the ester from step C (3.0 g, 7.7 mmol) in CH2Cl2 (10 mL) was added by double-tipped needle. The mixture was stirred a further 20 minutes, at which point it was poured into a mixture of 0.5M Na, K tartrate (150 mL) and ice (100 g). The product was extracted with EtOAc, and the organic layer was washed successively with 0.5M NaK tartrate, H2O, and brine. The solvent was then removed and yellow/orange oil (3.5 g) was used without purification in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05204344
Source datasetuspto-grants-1993_04
ORD IDord-e802a35896d6405697834146491bccc8
Source noteuspto-grants-1993_04