HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611599Generated: October 30, 2026
Hydrochloric Acid → 2-Formyl-3-thiopheneboronic acid
https://huagongshe.com/reaction/1611599
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-(3-Bromothiophen-2-yl)-1,3-dioxolane | HCID 12220211 | — |
| Reactant | n-Butylborate | HCID 86592051 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-Formyl-3-thiopheneboronic acid | HCID 2773426 | 50.2% |
Reaction Steps
A 1.1 N solution of n-butyllithium in hexane (28 ml). was added dropwise (10 mins) to a solution of 2-(3-bromo-2-thienyl)-1,3-dioxalane (3) (6.6 g, 28.1 mmol) in anhydrous ether (30 ml) at −70° C. After stirring for 10 mins, butyl borate (9.1 ml, 33.7 mmol) in anhydrous ether (20 ml) was added in a single portion. The reaction mixture was stirred for 4 hrs at −70° C. and then left to return to room temperature. 1 N hydrochloric acid (20 ml) was added, and the mixture was left for 1 hr with stirring. The aqueous phase was extracted with ether and the combined ether phases were washed with a solution of sodium bicarbonate, dried (Na2SO4), and evaporated under reduced pressure to give the intermediate (4) (2.2 g, 14.1 mmol, 50% yield) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06989388B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-9978e0d85b124f1ba62f54fcfba7ee84 |
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| Source note | uspto-grants-2006_01 |
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