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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908439Generated: October 28, 2026

Dichloromethane → (2-tert-butyl-5-nitro-1H-indol-7-yl)methanol

https://huagongshe.com/reaction/1908439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantMethyl 2-tert-butyl-5-nitro-1H-indole-7-carboxylateHCID 53436897—
SolventWaterHCID 962—
Product(2-tert-butyl-5-nitro-1H-indol-7-yl)methanolHCID 5912923573%

Reaction Steps

To a solution of methyl 2-tert-butyl-5-nitro-1H-indole-7-carboxylate (6.15 g, 22.3 mmol) and dichloromethane (30 ml) was added DIBAL-H (1.0 M, 20 mL, 20 mmol) at 78° C. The mixture was stirred for 1 h before water (10 mL) was added slowly. The resulting mixture was extracted with EtOAc (120 mL×3). The combined organic extracts were dried over anhydrous Na2SO4 and evaporated under vacuum to give (2-tert-butyl-5-nitro-1H-indol-7-yl)methanol (4.0 g, 73%), which was used in the next step directly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598181B2
Source datasetuspto-grants-2013_12
ORD IDord-2678f9b7c96442448fddf16d9a86ac89
Source noteuspto-grants-2013_12