HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719397Generated: October 30, 2026
Tetrahydrofuran → {2-[4-(2-Methyl-quinolin-4-ylmethoxy)-phenyl]-allyl}-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/719397
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1,2-Bis(diphenylphosphino)ethane | HCID 74267 | — |
| Reactant | 4-(4-Iodo-phenoxymethyl)-2-methylquinoline | HCID 21898059 | — |
| Reactant | (3-Trimethylsilanylallyl)-carbamic acid tert-butyl ester | HCID 85157761 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | {2-[4-(2-Methyl-quinolin-4-ylmethoxy)-phenyl]-allyl}-carbamic acid tert-butyl ester | HCID 69289521 | 14.8% |
Reaction Steps
THF (1.5 mL), Pd(OAc)2 (20 mg, 0.089 mmol, 8% eq) and 1,2-bis(diphenylphosphino)ethane (35.5 mg, 16% eq) were mixed under N2, degassed and stirred to give orange yellow mixture. A premixed solution of (3-trimethylsilanylallyl)-carbamic acid tert-butyl ester (250 mg, 1.09 mmol) from (7b) and 4-(4-iodo-phenoxymethyl)-2-methyl-quinoline (410 mg, 1.0 eq) from (7c) in benzene (3 ml) was added. The resulting mixture was heated at 50° C. over the weekend, then cooled to rt, diluted with ether, washed with water, dried and concentrated. {2-[4-(2-Methyl-quinolin-4-ylmethoxy)-phenyl]-allyl}-carbamic acid tert-butyl ester (65 mg, 14.8%) was obtained after the crude was purified by flash column chromatography (20%–40% ethyl acetate-hexanes). MS Found: (M+H)+=405.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07132432B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-991cca04f0504b0c842a52a6be25504a |
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| Source note | uspto-grants-2006_11 |
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