HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275135Generated: October 25, 2026
Water → Methyl 3-methoxy4-(5-nitrobenzo[b]thien-3-ylmethyl)benzoate
https://huagongshe.com/reaction/275135
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Methyl 4-(bromomethyl)-3-methoxybenzoate | HCID 2759828 | — |
| Reactant | 5-Nitro-1-benzothiophene | HCID 12414084 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-methoxy4-(5-nitrobenzo[b]thien-3-ylmethyl)benzoate | HCID 14763112 | — |
Reaction Steps
Stannic chloride (0.41 g.) was added to a stirred solution of 5-nitrobenzo[b]thiophene (0.28 g.) and methyl 4-bromomethyl-3-methoxybenzoate (B) (0.61 g.) in dichloromethane (5 ml.). The mixture was heated under reflux for 18 hours. The cooled mixture was poured into water (10 ml.) and extracted with dichloromethane (2×20 ml.). The combined extracts were dried (MgSO4) and evaporated. The oil was purified by flash chromatography on silica gel (100 ml.) eluting with 1:9 v/v ethyl acetate:hexane. The solid obtained was crystallized from hexane to give methyl 3-methoxy-4-(5-nitrobenzo[b]thien-3-ylmethyl)benzoate (I) as a solid (0.16 g., 30%); NMR: (250 MHz, CDCl3): 3.92(s, 3H, OCH3), 3.98(s,3H, OCH3), 4.28(s,2H, CH2 --Ar), 7.15 (d,1H), 7.22(s,1H), 7.56(m,2H), 7.93(d,1H), 8.19(dd, 1H); 8.73(d,1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05391758 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-369a7bbec6e046beb4ca9cbf490165aa |
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| Source note | uspto-grants-1995_02 |
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