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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305588Generated: October 31, 2026

Acetic Acid → HCID 22310861, compound

https://huagongshe.com/reaction/2305588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthyl oxoacetateHCID 70211—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 22310882HCID 22310882—
SolventMethanolHCID 887—
ProductHCID 22310861HCID 2231086167%

Reaction Steps

Sodium cyanoborohydride (0.2 g) was added in a single portion to methyl N-(3,4-dichlorobenzyl)-5-aminoindole-2-carboxylate (0.16 g), ethyl glyoxalate (0.2 ml of 50 wt % solution in toluene) and acetic acid (0.1 ml) in methanol (3 ml). The reaction was stirred for 5 mins then partitioned between ethyl acetate and 2M HCl. Combined organic extracts were dried (MgSO4) and concentrated to give an oil which crystallised upon trituration with i-hexane. Filtration yielded the desired end product as an off-white powder (0.136 g, 67%); NMR δ(CD3SOCD3) 1.18 (t, 3H), 3.79 (s, 3H), 3.82 (d, 2H), 4.08 (q, 2H), 5.72 (s, 2H), 6.60-7.50 (m, 7H); M/z (+) 435 (M+), 133.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441004B1
Source datasetuspto-grants-2002_08
ORD IDord-189944261a8b4d7f892a7c249c2d8f8f
Source noteuspto-grants-2002_08