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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593276Generated: November 4, 2026

Triethylamine → HCID 68604076, compound

https://huagongshe.com/reaction/1593276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-AminothiophenolHCID 8713—
ReactantHCID 86604631HCID 86604631—
SolventMethanolHCID 887—
ProductHCID 68604076HCID 68604076—

Reaction Steps

To a deoxygenated solution of methyl (2Z)-2-{[(benzyloxy)carbonyl]amino}-3-(3,4-dichlorophenyl)acrylate (10a) (2.17 g, 5.7 mmol) in anhydrous methanol (40 ml) (warmed to dissolve) under nitrogen was added the 2-aminothiophenol (3.1 ml, 28.5 mmol) followed by addition of triethylamine (400 ul, 2.85 mmol). The mixture stirred 3 days at ambient temperature, concentrated to ca. 10 mL, partitioned between cold 1N hydrochloric acid (75 mL) and ethyl acetate (100 mL). The organic phase was separated and consecutively washed with 1N hydrochloric acid (4×), dilute aqueous sodium bicarbonate and brine, dried, filtered and evaporated to give the title compound (10b) as an 4:1 mixture (erythro:threo) (2.8 g, 96%). A 100 mg sample was converted to the HCl salt to provide an analytically pure title compound (32 mg) as a (4:1) mixture. MS APCI, m/z=505 (M+1), 507 (M+3). LC/MS: 2.94 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07294622B2
Source datasetuspto-grants-2007_11
ORD IDord-a5f4371cf0b34f99b897c5e2075f9765
Source noteuspto-grants-2007_11