HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5616Generated: October 26, 2026
Acetic Acid → HCID 57299430, compound
https://huagongshe.com/reaction/5616
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1-benzyl-1H-indole-3-carbaldehyde | HCID 262104 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Methyl 2-(phenylamino)acetate hydrochloride | HCID 12241365 | — |
| Product | HCID 57299430 | HCID 57299430 | 43% |
Reaction Steps
To a suspension of methyl (+/-)-phenylglycinate hydrochloride (4.00 g, 19.8 mmol) in MeOH (50 mL), and HOAc (4 mL) was added 1-phenylmethyl-indole-3-carboxaldehyde (2.85 g, 12.1 mmol). The resulting mixture was allowed to stir at room temperature for 20 minutes; then NaBH3CN (1.98 g, 31.5 mmol) was added in one portion. The suspension was allowed to stir at room temperature for 18 hours, then was concentrated in vacuo to furnish a sticky white semi-solid. The crude reaction mixture was partitioned between 20% aqueous NaOH (0.25 L) and EtOAc (0.25 L); the organic phase was separated, washed with brine (0.25 L), and dried (Na2SO4). Concentration in vacuo afforded the crude product as a pale green oil which was purified by chromatography on a column of silica gel (230-400 mesh, 500 g, 70 mm o.d., EtOAc-hexanes 25:75, 400 mL fractions) using the flash technique. Fractions 8-13 were combined to provide 2.0 g (43%) of the title compound as a white solid. Recrystallization from EtOAc-hexanes provided white needles, m.p. 109°-110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05245046 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-c456b7da73ac4e6ca23b379fc52bb58b |
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| Source note | uspto-grants-1993_09 |
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