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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242890Generated: October 27, 2026

Tetrabutylammonium borohydride → HCID 68157058, compound

https://huagongshe.com/reaction/242890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium borohydrideHCID 169536—
ReactantHCID 86668874HCID 86668874—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68157058HCID 6815705882.1%

Reaction Steps

Tetrabutylammonium borohydride (800 mg, 3.10 mmol) was added at RT to a solution of 3-o-tolylbenzo[b]thiophene-2-carbaldehyde (2.07 mmol) in THF (10 mL) and IMS (1 mL) and the mixture stirred at RT for 1 h. The reaction mixture was quenched by addition of MeOH and volatiles were removed under reduced pressure. The resulting residues was purified by column chromatography (Si—PCC, gradient 0-30% EtOAc in cyclohexane) affording the title compound as an oil (432 mg, 82% over 2 steps). LCMS (Method C): RT 3.74 min [M-OH]+ 237.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-cba0b6f723a942f89638edc13dae137e
Source noteuspto-grants-2014_02