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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741191Generated: October 30, 2026

Methanol → Methyl-5-methoxy-3-aminovalerate

https://huagongshe.com/reaction/1741191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDichloromethaneHCID 6344—
ReactantMethyl 5-methoxy-3-oxopentanoateHCID 542416—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventHydrochloric AcidHCID 313—
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 formats (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) δ 1.25 (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 numberUS05973003
Source datasetuspto-grants-1999_10
ORD IDord-7cb49e4d96bd43dda4dd8ebe6ad7c14a
Source noteuspto-grants-1999_10