Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741192Generated: October 30, 2026

Methanol → HCID 21834683, compound

https://huagongshe.com/reaction/1741192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDimethyl acetylsuccinateHCID 112039—
ReactantAmmonium formateHCID 2723923—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventHydrochloric AcidHCID 313—
SolventDichloromethaneHCID 6344—
ProductHCID 21834683HCID 2183468359.8%

Reaction Steps

Dimethyl acetylsuccinate (10 g, 53 mmol) was added to methanol (200 ml) followed by ammonium formate (34 g, 530 mmol) and NaBH3CN (3.4 g, 53 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 dimethyl-2-(aminoethyl)succinate (6 g). 1H NMR (d6-DMSO) δ 0.97 (d, 3H, J=7.1 Hz), 2.66 (m, 2H), 3.05 (m, 1H), 3.56 (s, 3H), 3.60 (s, 3H), 4.15 (m, 1H); MS (FAB) m/z 190.2 (MH+), 158.2, 141.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05973003
Source datasetuspto-grants-1999_10
ORD IDord-4d5e456841594fdcac573eea1a32f5b6
Source noteuspto-grants-1999_10