HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195826Generated: November 2, 2026
Hydrochloric Acid → HCID 178419611, compound
https://huagongshe.com/reaction/1195826
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzo(B)Thiophene | HCID 7221 | — |
| Reactant | Magnesium Bromide | HCID 82241 | — |
| Reactant | N,N-bis(trimethylsilyl)-4-methoxy-2-butynylamine | HCID 13161121 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Nickel Dichloride | HCID 24385 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178419611 | HCID 178419611 | — |
Reaction Steps
2-Benzothiophenylmagnesium bromide was prepared by adding butyllithium (5.1 ml, 15.8 mM) to benzothiophene (1.7 g, 12.7 mM) in a 3-necked, 100 ml flask with septum, stir bar, thermometer, and nitrogen inlet, in the presence of ether (15 ml), allowing reaction to reflux about 15 minutes, and then cooling to 0° C. in ice. Magnesium bromide etherate (12.7 mM) was added all at once and was allowed to warm to 20° C. over about 15 minutes. Then NiCl2 (dppp) (30 mg) was added and, following the procedure described in Example 2, III (12.7 mM) was added and stirred overnight to produce the crude silylate product, the reaction being complete by G C analysis after that time. 1M ethanolic hydrochloride (0.9 equivalent), was added to the etheral solution to yield 1.7 g (72%) of hydrochloride salt as a pale yellow solid, Mp 235° C. (dec) (EtoH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05112852 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-a3133cf4ec984f0f8f8845b63ce0dd8c |
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| Source note | uspto-grants-1992_05 |
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