HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731073Generated: October 29, 2026
Potassium Hydroxide → HCID 11339826, compound
https://huagongshe.com/reaction/731073
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 68814951 | HCID 68814951 | — |
| Product | HCID 11339826 | HCID 11339826 | — |
Reaction Steps
The desired product was prepared using a procedure similar to step 2 of example 4. Thus, [4-(1-benzyl-3-methyl-2-phenyl-1H-indol-6-yl)-phenoxy]-acetic acid methyl ester (0.299 g, 0.648 mmol) was reacted with 1N KOH (1.3 ml) to give the product (0.231 g, 0.511 mmol, 79%) as a white solid, mp 202-205° C. 1H NMR (DMSO-d6) δ 2.23 (s, 3H), 4.68 (s, 2H), 5.39 (s, 2H), 6.86 (d, J=7.2 Hz, 2H), 6.96 (d, J=8.9 Hz, 2H), 7.13 (t, J=7.2 Hz, 1H), 7.18 (t, J=7.0 Hz, 2H), 7.34 (dd, J=1.4, 8.3 Hz, 1H), 7.39-7.44 (m, 3H), 7.49 (t, J=7.0 Hz, 2H), 7.56-7.61 (m, 4H); IR (solid) 3280, 2905, 1760, 1720, 1605, 1520, 1480, 1440, and 1240 cm1; [ESI(+)], m/z 448 (M+H)+; Anal. Calcd. for C30H25NO3.0.25H2O: C, 79.71; H, 5.57; N, 3.10; Found: C, 79.79; H, 5.66; N, 3.05.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582773B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-d354d3ea93684737ae9b81eb9f3a753f |
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| Source note | uspto-grants-2009_09 |
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