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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633657Generated: October 30, 2026

Lithium tri-s-butylborohydride → HCID 18679504, compound

https://huagongshe.com/reaction/1633657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium tri-s-butylborohydrideHCID 3611392—
ReactantHCID 18679488HCID 18679488—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18679504HCID 1867950496.5%

Reaction Conditions

Temperature75 °C

Reaction Steps

To 140 ml (140 mmol) 1M L-selectride in THF (Lithium-tri-sec-butylborohydride), 14.9 g (50 mmol) 1-(4-Bromo-phenyl)-5-methoxy-1H-indole were added slowly in small portions at RT. The mixture was stirred at 75° C. for 60 h, concentrated and dissolved in ether and water. The organic phase was washed with water and dried over Na2SO4. Trituration with cyclohexane yielded 13.9 g (96%) 1-(4-Bromo-phenyl)-1H-indol-5-ol as grey solid, MS: 287 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06503907B2
Source datasetuspto-grants-2003_01
ORD IDord-e5f26b2195344ce391faf306a50ffedc
Source noteuspto-grants-2003_01