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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721720Generated: October 31, 2026

Methyl bromoacetate → HCID 9934727, compound

https://huagongshe.com/reaction/1721720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl bromoacetateHCID 60984—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 9801388HCID 9801388—
SolventAcetonitrileHCID 6342—
ProductHCID 9934727HCID 9934727—

Reaction Steps

A solution of 150 mg (0.37 mmol) of the trans-isomer of (±)-2-(3,5-bis(trifluoromethyl)benzyloxy)-3-phenyl morpholine (Example 4) and 0.18 mL (1.00 mmol) of N,N-diisopropyl-ethyl- amine in 2 mL of acetonitrile was treated with 0.095 mL (1.00 mmol) of methyl bromoacetate and the resulting solution was stirred at rt for 20 h. The solution was concentrated in vacuo and the residue was partitioned between 20 mL of ethyl acetate and 5 mL of 0.5N aqueous potassium hydrogen sulfate solution. The layers were separated; the organic layer was washed with 10 mL of saturated aqueous sodium chloride solution, dried over magnesium sulfate and concentrated in vacuo. Flash chromatography on 10 g of silica gel using 4:1 v/v hexanes/ether as the eluant afforded 164 mg (93%) of the trans-isomer of the title compound as an oil: 1H NMR 2.79 (dr, 1 H, J=3.2, 11.2), 2.93 (dt, 1 H, J=11.2, 1.6), 3.52 (d, 1 H, J=7.2), 3.63 (s, 3 H), 3.92 (dt, 1 H, J=2.8, 11.6), 4.04 (ddd, 1 H, J=11.6, 3.2, 1.6), 4.45 and 4.84 (AB q, 2 H, J=13.2), 4.46 (d, 1 H, J=7.2), 7.31-7.38 (m, 6 H), 7.68 (s, 1 H);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05512570
Source datasetuspto-grants-1996_04
ORD IDord-7096f6d7166248348e7a623e6d03431f
Source noteuspto-grants-1996_04