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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621270Generated: November 2, 2026

HCID 68004074, compound → (1H-Indol-3-ylsulfanyl)-acetic acid

https://huagongshe.com/reaction/1621270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68004074HCID 68004074—
SolventLithium HydroxideHCID 3939—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product(1H-Indol-3-ylsulfanyl)-acetic acidHCID 59070738%

Reaction Steps

Methyl 2-((1H-indol-3-yl)thio)acetate from Step A was dissolved in a mixture of tetrahydrofuran (20 mL) and 2.0 M aqueous LiOH (15 mL), then stirred vigorously at ambient temperature for 30 min. Tetrahydrofuran was removed in vacuo, the aqueous layer neutralized with 1.2 N HCl and extracted with CH2Cl2. The organic layer was dried over magnesium sulfate and the solvent was removed in vacuo to produce an oily residue. Upon diluting the residue in dichloromethane a solid formed which was filtered and dried to yield the desired product (2.00 grams, 9.65 mmol, 38% yield over 2 steps). LCMS>99% at 254 nm, RT=1.02 min, m/z=208 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772509B2
Source datasetuspto-grants-2014_07
ORD IDord-7081289dd766440c83c3699322d7769c
Source noteuspto-grants-2014_07