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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011647Generated: October 31, 2026

Acetic acid, phosphono-, 1-(1,1-dimethylethyl) ester, diammonium salt → HCID 67313493, compound

https://huagongshe.com/reaction/1011647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid, phosphono-, 1-(1,1-dimethylethyl) ester, diammonium saltHCID 431492—
ReactantEthyl 6-formylbenzo[b]thiophene-2-carboxylateHCID 57443969—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67313493HCID 6731349371%

Reaction Steps

To a stirred solution of tert-butyl phosphonoacetate (1.7 g, 7.27 mmol) in THF (20 mL) was slowly added n-butyllithium (1.6 M, 5 mL) with cooling to −78 degrees Celsius. After stirring for 30 minutes at −78 degrees Celsius, this solution was added into a solution of 6-formyl-benzo[b]thiophene-2-carboxylic acid ethyl ester (1.83 g, 7.27 mmol). The resulting solution was stirred at −78 degrees Celsius for 30 minutes before being allowed to warm to room temperature. The solution was subsequently cooled back to −78 degrees Celsius and quenched with sat. aq NH4Cl. The mixture was extracted with ethyl acetate, and the combined organic extracts were dried over anhydrous sodium sulfate. After being filtrated and concentrated, the residue was purified by flash column chromatography to give 1.7 g (71%) of 6-(2-tert-butoxycarbonyl-vinyl)-benzo[b]thiophene-2-carboxylic acid ethyl ester. MS: calc'd 333 (MH+), exp 333 (MH+). 1H NMR (d6-DMSO, 400 MHz), 8.38 (s, 1H), 8.18 (s, 1H), 8.02 (d, 1H, J=8.4 Hz), 7.82 (d, 1H, J=8.4 Hz), 7.66 (d, 1H, J=16.0 Hz), 6.66 (d, 1H, J=16.0 Hz), 4.36 (q, 2H, J=7.2 Hz), 1.49 (s, 9H), 1.34 (t, 3H, J=7.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977372B2
Source datasetuspto-grants-2011_07
ORD IDord-a5975a060a4648df9f6d7125da400db6
Source noteuspto-grants-2011_07