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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767298Generated: November 3, 2026

4-Methylmorpholine → HCID 21113522, compound

https://huagongshe.com/reaction/1767298

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-Chloro-2-Methylpropyl ChloroformateHCID 2733326—
ReactantBenzyl 3-(aminomethyl)-5-methylhexanoate hydrochlorideHCID 21113525—
SolventDichloromethaneHCID 6344—
ProductHCID 21113522HCID 21113522—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of (39) (594 mg, 2.38 mmol) in dichloromethane at 0° C. was added N-methylmorpholine (0.523 mL, 4.77 mmol) and 1-chloro-2-methylpropyl chloroformate (0.347 mL, 2.38 mmol). The resulting solution was stirred at 0° C. until the reaction was complete (˜30 min, as monitored by TLC) and then was diluted with dichloromethane, washed successively with cold 1N HCl solution, water and brine, then dried over anhydrous Na2SO4. Filtration and removal of the solvent in vacuo afforded the title compound (42) as a mixture of two diastereomers (840 mg, 92%), which was used without further purification in the following example. 1H-NMR (CDCl3, 400 MHz): δ 0.86 (2 d, 6H), 1.02 (2 d, 6H), 1.15 (m, 2H), 1.63 (m, 1H), 2.14 (m, 2H), 2.34 (m, 2H), 3.10 (m, 1H), 3.28 (m, 1H), 5.11 (br.s, 3H), 6.29 (d, 1H), 7.31 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07232924B2
Source datasetuspto-grants-2007_06
ORD IDord-bc7c44a242fa478ca72a674705904271
Source noteuspto-grants-2007_06