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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261759Generated: November 2, 2026

Trimethylsilyldiazomethane → Methyl 6-Bromo-1H-Indole-3-Carboxylate

https://huagongshe.com/reaction/2261759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant6-Bromo-1H-indole-3-carboxylic acidHCID 15284837—
SolventMethanolHCID 887—
ProductMethyl 6-Bromo-1H-Indole-3-CarboxylateHCID 11499811100%

Reaction Steps

To a solution of 6-bromoindole-3-carboxylic acid (960 mg, 4.00 mmol) in methanol (9.5 mL) is added (trimethylsilyl)diazomethane (2.0 M solution in hexanes, approximately 9 mL) over two minutes at room temperature. The yellow mixture is concentrated under reduced pressure. The residue is redissolved in methanol and concentrated under reduced pressure several times to give the title compound as a solid (100%). ES/MS m/e 256.0 (M+2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846960B2
Source datasetuspto-grants-2010_12
ORD IDord-e1f15c8edef84905b3ff6b3440d6ca97
Source noteuspto-grants-2010_12