Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877008Generated: October 31, 2026

Ammonium Chloride → HCID 68511351, compound

https://huagongshe.com/reaction/1877008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 5-bromo-2-ethylthiophene-3-carboxylateHCID 68515411—
ReactantHCID 178420663HCID 178420663—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68511351HCID 6851135180%

Reaction Steps

To a solution of ethyl 5-bromo-2-ethylthiophene-3-carboxylate (5.00 g) synthesized in Example 69 (4) in tetrahydrofuran (50 mL) was added dropwise 1.0M isopropylmagnesium bromide-tetrahydrofuran solution (28.5 mL) at −40° C., and the mixture was stirred for 1.5 hr under an argon atmosphere. Isobutylaldehyde (8.67 mL) was added dropwise, and the mixture was stirred at −40° C. for 1 hr and at room temperature for 1 hr. Saturated aqueous ammonium chloride solution was added to quench the reaction, and the mixture was extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. To a solution of the residue in trifluoroacetic acid (50 mL) was added triethylsilane (9.10 mL), and the mixture was stirred at room temperature for 3 hr, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:24, volume ratio) to give the title compound (3.67 g, 80%) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309580B2
Source datasetuspto-grants-2012_11
ORD IDord-522caf57114640d28f36f0a9b59bf312
Source noteuspto-grants-2012_11