HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889183Generated: October 30, 2026
4-Methyloxybenzyl chloride → HCID 59610063, compound
https://huagongshe.com/reaction/1889183
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methyloxybenzyl chloride | HCID 69993 | — |
| Reactant | tert-butyl N-(5-bromo-1,3-thiazol-2-yl)carbamate | HCID 21300388 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59610063 | HCID 59610063 | — |
Reaction Steps
To a single necked round bottom flask (5-Bromo-thiazol-2-yl)-carbamic acid tert-butyl ester (1.4 g, 5.01 mmol) was dissolved in 25 ml dry DCM. To it 1,8-Diazabicyclo[5.4.0]undec-7-ene(DBU) (2.24 ml, 15.03 mmol) was added followed by 1-Chloromethyl-4-methoxy-benzene (1.02 ml, 7.52 mmol) addition was done and reaction mixture was stirred for overnight. Reaction was quenched by addition of water (20 ml), extracted with DCM (25 ml), Organic layer was separated and washed with brine (30 ml) and dried over anhydrous sodium sulfate, sodium sulfate was filtered and washed with DCM (20 ml) and solvent was evaporated on rotavapour to get required product. The crude material was purified by silica-gel column chromatography, eluting with 4% acetone in hexane. (1.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501955B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-5ecb4a5a5f2b471eaed0aaed490c6fa7 |
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| Source note | uspto-grants-2013_08 |
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