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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307875Generated: November 1, 2026

Isothiocyanatotrimethylsilane → (8-Thiocyanato-chroman-5-yloxy)-acetic acid methyl ester

https://huagongshe.com/reaction/2307875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsothiocyanatotrimethylsilaneHCID 75297—
Reactant(Chroman-5-yloxy)-acetic acid methyl esterHCID 11322001—
ReactantHCID 178525681HCID 178525681—
Solvent1,1,1,3,3,3-Hexafluoro-2-propanolHCID 13529—
Product(8-Thiocyanato-chroman-5-yloxy)-acetic acid methyl esterHCID 1119672850%

Reaction Steps

A stirred solution of (chroman-5-yloxy)-acetic acid methyl ester (2.1 g, 9.4 mmol) and trimethylsilyl isothiocyanate (2 mL, 14.1 mmol) in 30 mL 1,1,1,3,3,3-hexafluoro-propan-2-ol under a N2 atmosphere was treated with phenyliodine(III) bis(trifluoroacetate). The reaction mixture stirred at room temperature for 1 h and concentrated in vacuo. Purification by flash column chromatography (gradient elution: 10% EtOAc/hexanes to 40% EtOAc/hexanes) gave the title compound (1.3 g, 50%) as a pale yellow solid. 400 MHz 1H NMR (DMSO-d6) δ 7.31 (d, 1H, J=8.8 Hz), 6.54 (d, 1H, J=8.8 Hz), 4.83 (s, 2H), 4.21 (t, 2H, J=4.9 Hz), 3.64 (s, 3H), 2.60 (t, 2H, J=6.4 Hz), 1.89 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06833380B2
Source datasetuspto-grants-2004_12
ORD IDord-e73c6d3bb5894f8a84eec94f1205614c
Source noteuspto-grants-2004_12