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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298627Generated: October 25, 2026

3-(Bromoacetyl)-5-t-butyl-2-methyl-furan → HCID 86583822, compound

https://huagongshe.com/reaction/2298627

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Bromoacetyl)-5-t-butyl-2-methyl-furanHCID 12025898—
ReactantMethyl 4-(aminothioxomethyl)-5-methylthiothiophene-2-carboxylateHCID 86583815—
ProductHCID 86583822HCID 8658382266.1%

Reaction Steps

A solution of 955 mg (3.86 mmol) of methyl 4-(aminothioxomethyl)-5-methylthiothiophene-2-carboxylate (Maybridge, Cornwall, UK) was reacted with 1 g (3.86 mmol) of 1-[5-(tert-butyl)-2-methyl(3-furyl)]-2-bromoethan-1-one (1 g) in a manner similar to Example 8, step (a) to give methyl 4-{4-[5-(tert-butyl)-2-methyl(3-furyl)](1,3-thiazol-2-yl)}-5-methylthiothiophene-2-carboxylate (999 mg, 64%) as a red-brown solid. 1H-NMR (DMSO-d6; 300 MHz) δ8.14 (s, 1H), 7.74 (s, 1H), 6.46 (s, 1H), 3.86 (s, 3H), 2.74 (s, 3H), 2.66 (s, 3H), 1.27 (s, 9H). Mass spectrum (MALDI-TOF, CHCA matrix, m/z): Calcd. for C19H21NO3S3, 408.1 (M+H), found 408.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492403B1
Source datasetuspto-grants-2002_12
ORD IDord-623e5aa04f994e378d4c86a240182a0b
Source noteuspto-grants-2002_12