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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252055Generated: November 1, 2026

Tetrahydrofuran → 5-(2-Hydroxy-ethyl)-indole-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/252055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
Reactanttert-Butyl 5-ethenyl-1H-indole-1-carboxylateHCID 66890900—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-(2-Hydroxy-ethyl)-indole-1-carboxylic acid tert-butyl esterHCID 6689086176%

Reaction Steps

To a solution of 5-vinyl-indole-1-carboxylic acid tert-butyl ester (4.5 g, 18.5 mmol, 1.0 eq.) in THF (46 mL) at 0° C. was added 9-BBN (0.5 M in THF, 87 mL, 2.4 eq.) over 10 min. The resulting reaction mixture was stirred for 2.5 h and diluted with THF (150 mL) and water (150 mL) while keeping the temperature at 0° C. Then NaBO3.4H2O (44 g) was introduced and resulting reaction mixture was stirred and warmed to room temperature and stirred. The reaction mixture was diluted with methylene chloride (100 mL) and the separated aqueous layer was extracted 3×100 mL methylene chloride. The combined organic layers were dried over sodium sulfate, filtered and concentrated. The residue was purified by chromatography (methylene chloride to 5% acetone/methylene chloride) to give 5-(2-hydroxy-ethyl)-indole-1-carboxylic acid tert-butyl ester (3.82 g, 76%) or similarly 6-(2-hydroxy-ethyl)-indole-1-carboxylic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868002B2
Source datasetuspto-grants-2011_01
ORD IDord-69d8ff96af1f4fc18fd40622c5b022b0
Source noteuspto-grants-2011_01