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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747232Generated: October 31, 2026

4-Methylmorpholine → HCID 131733559, compound

https://huagongshe.com/reaction/1747232

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantSodium borohydrideHCID 4311764—
ReactantN-(tert-Butoxycarbonyl)-3-iodo-D-phenylalanineHCID 46737391—
SolventTetrahydrofuranHCID 8028—
SolventDimethylacetamideHCID 31374—
ProductHCID 131733559HCID 131733559—

Reaction Steps

A solution of Boc-3-iodo-D-phenylalanine (6.32 g, 16.2 mmol) and 4-methyl-morpholine (1.87 ml, 17 mol) in THF (13 mL) was added dropwise to a −15° C. solution of isobutyl chloroformate (2.22 mL, 17 mmol) in THF (13 mL) and the resulting suspension was stirred for 1 h. The cold reaction mixture was filtered and the filter cake was rinsed with THF. The filtrate was added dropwise to a 0° C. solution of NaBH4 (0.92 g, 24.2 mmol) in dimethylacetamide (7 mL) and the resulting suspension was warmed to RT and stirred for 1 h. The reaction mixture was cooled back to 0° C. and quenched with 1M aq. citric acid. Additional water was added and the mixture was concentrated in vacuo. The remaining aqueous phase was acidified with 1M aq. HCl before being filtered. The filter cake was rinsed with water and dried under HV to give the title compound as an orange solid that was used further without purification. LC-MS A: tR=0.84 min; [M-Me]+=362.93.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150566B2
Source datasetuspto-grants-2015_10
ORD IDord-ec55187e56e14069b56276fd51674f50
Source noteuspto-grants-2015_10