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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206557Generated: October 31, 2026

Sodium borohydride → HCID 117778794, compound

https://huagongshe.com/reaction/2206557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 89740097HCID 89740097—
SolventTetrahydrofuranHCID 8028—
ProductHCID 117778794HCID 11777879493%

Reaction Steps

To a mixture of tert-butyl 2-methyl-1-(3-oxobutan-2-yl)-1H-indole-3-carboxylate (120 mg, 0.39 mmol) in tetrahydrofuran (3 mL) was added sodium borohydride (79 mg, 2.08 mmol). The reaction mixture was stirred at room temperature for 3 hours. The reaction mixture was quenched by adding water (3 ml) and extracted with ethyl acetate (20 mL×4). The combined organic layers was dried over sodium sulfate and concentrate to afford tert-butyl 1-(3-hydroxybutan-2-yl)-2-methyl-1H-indole-3-carboxylate (110 mg, yield: 93%) as a yellow oil. LRMS (M+H+) m/z: calcd 303.17. found 304.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371331B2
Source datasetuspto-grants-2016_06
ORD IDord-6fa3a91ac5ca4cfb9be635b9ef0760ef
Source noteuspto-grants-2016_06