HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086550Generated: October 30, 2026
Water → Methyl 4-(5-hexanamidobenzo[b]thien-3-ylmethyl)-3methoxybenzoate
https://huagongshe.com/reaction/1086550
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Hexanoyl chloride | HCID 67340 | — |
| Reactant | Methyl 4-(5-aminobenzo[b]thien-3-ylmethyl)-3-methoxybenzoate | HCID 14763113 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 4-(5-hexanamidobenzo[b]thien-3-ylmethyl)-3methoxybenzoate | HCID 23365890 | 75% |
Reaction Steps
Hexanoyl chloride (0.024 g.) was added to a stirred solution of methyl 4-(5-aminobenzo[b]thien-3-ylmethyl)-3-methoxybenzoate (H) (0.06 g.), and N-methylmorpholine (0.1 ml.) in dichloromethane (3 ml.). The mixture was stirred for 1 hour and then poured into water (20 ml.). The aqueous mixture was extracted with dichloromethane (2×20 ml.). The combined extracts were dried (MgSO4), and evaporated. The mixture was recrystallized from a mixture of ethyl acetate and hexane to give the title compound (0.05 g., 75%) as a colorless solid: NMR (250 MHz, DMSO-d6): 0.87(t,3H, CH2CH3), 1.28(m,4H, CH2.CH2.CH3), 1.59 (quintet,2H, CH2CH2CON), 2.29(t,2H, CH2CON), 3.84(s, 3H, OCH3), 3.91(s,3H, OCH3), 4.11(s,2H, CH2 --Ar), 7.14 (d,1H), 7.34(s, 1H), 7.49(m,3H), 7.86(d,1H), 8.11(d, 1H), 9.95(s,1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05030643 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-70f272fa215f4c6ba1bfede3a8d68e12 |
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| Source note | uspto-grants-1991_07 |
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