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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5616Generated: October 26, 2026

Acetic Acid → HCID 57299430, compound

https://huagongshe.com/reaction/5616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethanolHCID 887—
Reactant1-benzyl-1H-indole-3-carbaldehydeHCID 262104—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantMethyl 2-(phenylamino)acetate hydrochlorideHCID 12241365—
ProductHCID 57299430HCID 5729943043%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05245046
Source datasetuspto-grants-1993_09
ORD IDord-c456b7da73ac4e6ca23b379fc52bb58b
Source noteuspto-grants-1993_09