HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651263Generated: October 27, 2026
3-Methoxythiophenolate → HCID 14742775, compound
https://huagongshe.com/reaction/1651263
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Methoxythiophenolate | HCID 6950198 | — |
| Reactant | 1-Bromoheptan-2-one | HCID 12431734 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14742775 | HCID 14742775 | 99.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04927838 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-062a09d3f46b49808bc191b43b888115 |
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| Source note | uspto-grants-1990_05 |
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