HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298639Generated: October 29, 2026
3-Hydroxyphenacyl bromide → HCID 18537150, compound
https://huagongshe.com/reaction/2298639
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Hydroxyphenacyl bromide | HCID 6917206 | — |
| Reactant | HCID 18537366 | HCID 18537366 | — |
| Product | HCID 18537150 | HCID 18537150 | — |
Reaction Steps
A solution of 1.97 g (8.1 mmol) of isopropyl 4-(aminothioxomethyl)-5-methylthiophene-2-carboxylate was reacted with 1.74 g (8.1 mmol) of 3′-hydroxy-2-bromoacetophenone (Example 40, step (a)) were reacted in a manner similar to Example 8, step (a) to give, after column chromatography on silica gel eluting with hexane:ethyl acetate 7/3 (v:v), crystallization from acetonitrile, and recrystallization from hexanes, isopropyl 4-[4-(3-hydroxyphenyl)(1,3-thiazol-2-yl)]-5-methylthiophene-2-carboxylate (1.4 g, 48%) as brown solid. 1H-NMR (DMSO-d6; 300 MHz) δ9.57 (br s, 1H), 8.14 (s, 1H), 8.08 (s, 1H), 7.46 (m, 2H), 7.26 (m, 1H), ), 6.78 (m, 1H), 5.12 (septet, 1H, J=6.2 Hz), 2.85 (s, 3H), 1.33 (d, 6H, J=6.2 Hz). Mass spectrum (ESI, m/z): Calcd. for C18H17NO3S2 360.1 (M+H), found 360.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06492403B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-e0d3357d1d3345baa816552abe787214 |
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| Source note | uspto-grants-2002_12 |
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