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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754263Generated: October 31, 2026

Tetrahydrofuran → HCID 86707748, compound

https://huagongshe.com/reaction/1754263

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 sat′d 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 R1a (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 numberUS09169240B2
Source datasetuspto-grants-2015_10
ORD IDord-96be531249ce4fb382c9c88e26f55314
Source noteuspto-grants-2015_10