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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1190854Generated: November 3, 2026

Tetrahydrofuran → HCID 86707748, compound

https://huagongshe.com/reaction/1190854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantMethyl propionateHCID 11124—
Reactant6-Bromo-2-chlorobenzothiazoleHCID 2049871—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
SolventTolueneHCID 1140—
ProductHCID 86707748HCID 8670774874%

Reaction Steps

To a solution of methyl propionate (0.088 mL, 0.89 mmol) and 6-bromo-2-chlorobenzo[d]thiazole (221 mg, 0.89 mmol) in degassed toluene (5 mL) at brine/ice bath temperature was slowly added 1.0 M NaHMDS in THF (2.22 mL, 2.22 mmol). After the addition was complete, the reaction was stirred for 10 min. The mixture was then quenched with satd. NH4Cl (15 mL) then extracted with EtOAc (2×20 mL). The organic extracts were dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by silica gel chromatography eluting with 0-100% EtOAc/hexane to give Compound R3a (198 mg, 0.66 mmol, 74% yield) as a yellow solid. LCMS=1.0 min using analytical method (M), 302.0 (M+H). 1H NMR (400 MHz, CDCl3) δ 8.02 (d, J=1.8 Hz, 1H), 7.87 (d, J=8.8 Hz, 1H), 7.58 (dd, J=8.7, 1.9 Hz, 1H), 4.30 (q, J=7.3 Hz, 1H), 3.78 (s, 3H), 1.75 (d, J=7.3 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680090B2
Source datasetuspto-grants-2014_03
ORD IDord-8aebacdb23324f089ebf3bb8e1cb5d26
Source noteuspto-grants-2014_03