HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067206Generated: November 1, 2026
1-(Bromomethyl)-2,4-difluorobenzene → HCID 22557094, compound
https://huagongshe.com/reaction/1067206
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(Bromomethyl)-2,4-difluorobenzene | HCID 90297 | — |
| Reactant | (R)-2-tert-butoxycarbonylamino-3-hydroxy propionic acid | HCID 637603 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22557094 | HCID 22557094 | 71% |
Reaction Steps
To a solution of N-Boc-(D)-serine (452 9, 2.2026 mol) in a mixture of THF (7 L) and DMF (3 L) at about 0° C. was added potassium tert-butoxide solution (515.8 g, 4.5963 mol). The reaction mixture was stirred at about 0° C. for about 30 min., then 2,4-difluorobenzyl bromide (456.5 g, 2.2051 mol) was added. After warming to room temperature, the reaction mixture was concentrated in vacua to remove the THF. Partitioned the reaction mixture between 4.5 L H2O and 4.5 L IPE. Separated the layers and adjusted the pH of the aqueous layer with 1 N HCl to about 3. The aqueous layer was extracted twice with 4 L each of IPE. The organic solution was dried over Na2SO4, and concentrated in vacuo to yield a yellow waxy solid (518.0 g, yield: 70.9 %). 1H-NMR (CDCl3) δ1.44 (s, 9H), 3.73 (m, 1H), 3.94 (d, 1H), 4.44 (br s, 1H), 4.54 (s, 2H), 5.34 (m, 1H), 6.78 (m, 1H), 6.84 (m, 1H), 7.30 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06248717B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-501db7101d8f40dd8fa3e4739b11e789 |
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| Source note | uspto-grants-2001_06 |
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