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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294610Generated: October 30, 2026

Trifluoroacetic acid → 5-(3,4-Dimethoxy-phenyl)-thiomorpholine-3-carboxylic acid methyl ester

https://huagongshe.com/reaction/1294610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-Tert-butoxycarbonylamino-3-[2-(3,4-dimethoxy-phenyl)-2-oxo-ethylsulfanyl]-propionic acid methyl esterHCID 69156042—
SolventDichloromethaneHCID 6344—
Product5-(3,4-Dimethoxy-phenyl)-thiomorpholine-3-carboxylic acid methyl esterHCID 65171377—

Reaction Steps

To an ice chilled solution of 2-tert-butoxycarbonylamino-3-[2-(3,4-dimethoxy-phenyl)-2-oxo-ethylsulfanyl]-propionic acid methyl ester (2.00 g, 9.34 mmol, 1.0 equivalents) in dichloromethane (9 ml) was added trifluoroacetic acid (9 ml). The reaction solution was stirred on ice for 4 hours. The solution was concentrated, coevaporated with toluene. The residue was dissolved in dichloromethane (30 ml) and chilled on ice. To this was added sodium triacetoxyborohydride (2.97 g, 14.02 mmol, 1.5 equivalents) followed by dichloromethane (7 ml). The reaction was stirred 18 hours at room temperature. Saturated sodium bicarbonate was added, and the reaction mixture was extracted with dichloromethane. The dichloromethane extracts were dried with MgSO4, filtered and concentrated. 5-(3,4-Dimethoxy-phenyl)-thiomorpholine-3-carboxylic acid methyl ester was obtained as an oil (1.63 g, 59% yield). Analysis H1 NMR (400 MHz, CDCl3): 6.92 (2H, m), 6.83 (1H, d), 3.95 (3H, s), 3.93 (3H, s), 3.87 (2H, m), 3.85 (3H, s), 2.77 (3H, m), 2.42 (1H, m). MS (LC-MS): Calculated for C14H19NO4S 297.10. Found 298.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241765B2
Source datasetuspto-grants-2007_07
ORD IDord-8751cb8b5cac492599ad7a498577af33
Source noteuspto-grants-2007_07