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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651263Generated: October 27, 2026

3-Methoxythiophenolate → HCID 14742775, compound

https://huagongshe.com/reaction/1651263

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxythiophenolateHCID 6950198—
Reactant1-Bromoheptan-2-oneHCID 12431734—
SolventWaterHCID 962—
ProductHCID 14742775HCID 1474277599.9%

Reaction Steps

To a stirred solution of 3-methoxythiophenolate (45 g) in water (100 mL) at 15° C. was added dropwise over 20 minutes 1-bromo-2-heptanone (54.4 g). The reaction was stirred for 1 hour at room temperature then was extracted with diethyl ether (2×250 mL) and the ether extracts were washed in turn with water (2×100 mL) and 1N hydrochloric acid (2×100 mL). The dried (MgSO4) organic layers were combined and evaporated to yield crude 1-(3-methoxyphenylthio)-2-heptanone (71 g). The crude 1-(3-methoxyphenylthio)-2-heptanone (65 g) was added over 30 minutes with stirring to sulfuric acid at -10° C. After 30 minutes at -5° C., the reaction mixture was diluted carefully with ice (200 g) and the resulting solid was filtered off, washed with water and dried. Crystallization of the crude product from hexane gave 18.4 g of 6-methoxy-3-pentylbenzo[b]thiophene, mp 43°-45° C. A small sample was recrystallized from hexane to provide the analytical specimen, mp 45°-47° C. Anal. Calcd for C14H18OS: C, 71.75; H, 7.74; S, 13.68 Found: C, 71.81; H, 7.60; S, 13.37

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04927838
Source datasetuspto-grants-1990_05
ORD IDord-062a09d3f46b49808bc191b43b888115
Source noteuspto-grants-1990_05