HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235097Generated: October 31, 2026
Ammonium Hydroxide → HCID 68701783, compound
https://huagongshe.com/reaction/2235097
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Methyl 4-methoxy-1H-indole-6-carboxylate | HCID 12140116 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 68701783 | HCID 68701783 | 70% |
Reaction Steps
Sodium cyanoborohydride (3.6 g, 57.8 mmol, 3 equiv.) was added to a stirred solution of 4-methoxy-1H-indole-6-carboxylic acid methyl ester (3.96 g, 19.3 mmol, 1 equiv.) in acetic acid (40 mL) at room temperature over 5 minutes. The mixture was stirred for 30 minutes, then cooled to 0° C. and slowly poured onto concentrated ammonium hydroxide (78 mL, d=0.880) at 0° C. The mixture was diluted with water (20 mL) extracted with dichloromethane (4×25 mL). The organic layers were combined, dried over Na2SO4 and the solvent was removed under vacuum. The crude mixture was purified by flash column chromatography (SiO2, dichloromethane) and the fractions combined to afford 4-methoxy-2,3-dihydro-1H-indole-6-carboxylic acid methyl ester, 2.8 g (70% yield). LC @215 nm; Rt 0.85: 97%, m/z (ES+): 208 (M+H+.); δH (400 MHz; d6-DMSO) 6.90 (1H, s), 6.86 (1H, s), 3.80 (3H, s), 3.79 (3H, s), 3.49 (2H, t), 2.89 (2H, t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07713996B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-da585ef13b844494bec938c68e75ebd3 |
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| Source note | uspto-grants-2010_05 |
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