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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231558Generated: November 4, 2026

Hydrochloric Acid → HCID 178419611, compound

https://huagongshe.com/reaction/231558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzo(B)ThiopheneHCID 7221—
ReactantMagnesium BromideHCID 82241—
ReactantN,N-bis(trimethylsilyl)-4-methoxy-2-butynylamineHCID 13161121—
ReactantButyllithiumHCID 178418339—
CatalystNickel DichlorideHCID 24385—
SolventDiethyl EtherHCID 3283—
ProductHCID 178419611HCID 178419611—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04847288
Source datasetuspto-grants-1989_07
ORD IDord-bc075e3dbe014a0ab69b722b1c1864ef
Source noteuspto-grants-1989_07