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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225970Generated: November 2, 2026

Methanol → Diethyl-3-aminoadipate

https://huagongshe.com/reaction/2225970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDiethyl 3-oxoadipateHCID 81576—
ReactantAmmonium formateHCID 2723923—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventHydrochloric AcidHCID 313—
SolventDichloromethaneHCID 6344—
ProductDiethyl-3-aminoadipateHCID 2183472075%

Reaction Steps

Diethyl-3-oxoadipate (10 g, 46 mmol) was added to methanol (225 ml) followed by ammonium formate (27.4 g, 460 mmol) and NaBH3CN (2.7 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 was 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 diethyl-3-aminoadipate (7.5 g). 1H NMR (d6-DMSO) δ 1.25 (t, 3H, J=8 Hz), 1.26 (t, 3H, J=8 Hz), 1.8 (m,2H), 1.55 (bs, 2H), 3.18 (m, 1H), 4.13 (q, 4H, J=8 Hz), 4.15 (q, 4H, J=8 Hz); MS (FAB) m/z 218.3 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344957
Source datasetuspto-grants-1994_09
ORD IDord-3cbc10aee4274569ba2eb2a1facc4711
Source noteuspto-grants-1994_09