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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic acid, phosphono-, 1-(1,1-dimethylethyl) ester, diammonium salt | HCID 431492 | — |
| Reactant | Ethyl 6-formylbenzo[b]thiophene-2-carboxylate | HCID 57443969 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67313493 | HCID 67313493 | 71% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977372B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-a5975a060a4648df9f6d7125da400db6 |
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| Source note | uspto-grants-2011_07 |
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