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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253043Generated: November 2, 2026

Dimethylformamide → (R)-2-(3-formyl-benzyl)-morpholine-4-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2253043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAmmonium ChlorideHCID 25517—
ReactantN-Boc-(R)-2-(3-bromobenzyl)morpholineHCID 67073309—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
Product(R)-2-(3-formyl-benzyl)-morpholine-4-carboxylic acid tert-butyl esterHCID 8660706243%

Reaction Steps

The solution of 1.3 g (3.6 mmol) (R)-2-(3-bromo-benzyl)-morpholine-4-carboxylic acid tert-butyl ester in 80 mL diethyl ether was cooled down to −100° C. and treated dropwise with 2.6 mL (3.9 mmol; 1.5M solution in n-pentane) tert-butyllithium. After 15 min. 0.31 mL (4.0 mmol) N,N-dimethylformamide were added and the reaction stirred for another 1.5 h. The solution was poured on 10% aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, filtered and evaporated. The residue was chromatographed on silica gel with n-hexane:ethyl acetate (2:1 v/v) as eluant to give the desired compound as colorless oil (43%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323466B2
Source datasetuspto-grants-2008_01
ORD IDord-331b8b1e0314441988ee17a142a05b03
Source noteuspto-grants-2008_01