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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941553Generated: November 3, 2026

Methanol → Methyl-5-methoxy-3-aminovalerate

https://huagongshe.com/reaction/1941553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethyl 5-methoxy-3-oxopentanoateHCID 542416—
ReactantAmmonium formateHCID 2723923—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventHydrochloric AcidHCID 313—
SolventDichloromethaneHCID 6344—
ProductMethyl-5-methoxy-3-aminovalerateHCID 21834688101.1%

Reaction Steps

Methyl-5-methoxy-3-oxovalerate (10 g, 62.5 mmol) was added to methanol (200 ml) followed by ammonium formate (39.4 g, 620 mmol) and NaBH3CN (3.9 g, 46 mmol) at 25° C. After 24 h the methanol was removed in vacuo to leave a white mass. Methylene chloride was added and the mixture filtered. The methylene chloride was evaporated resulting in an oil which was dissolved in 1N HCl (200 ml) and extracted with ether (100 ml). The ether layer was discarded and the aqueous layer was made basic using solid K2CO3. The product was extracted into methylene chloride dried over Na2SO4 and evaporated to give methyl-5-methoxy-3-aminovalerate (7.5 g). 1H NMR (d6 -DMSO) δ1.25 (m, 3H) 1.66 (m, 2H), 1.86 (bs, 2H), 2.9 (M, 2H), 3.33 (s, 3H), 3.49 (M, 2H), 3.7 (s, 3H); MS (FAB) m/z 161.2 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05703125
Source datasetuspto-grants-1997_12
ORD IDord-1bfbb0029a7d449c8ded359a1a09d9d5
Source noteuspto-grants-1997_12