HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-4-iodobutane → 6-Chloro-2-(2,4-difluorophenyl)hexanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-4-iodobutane | HCID 82527 | — |
| Reactant | 2,4-Difluorophenylacetic acid | HCID 123581 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Product | 6-Chloro-2-(2,4-difluorophenyl)hexanoic acid | HCID 58110087 | 89% |
Reaction Steps
Step AM (1): 2-(2,4-Difluorophenyl)acetic acid (2.5 g, 14.52 mmol) was deprotonated with NaHMDS (1.0 M in THF, 29.0 mL, 29.0 mmol) and reacted with 1-chloro-4-iodobutane (1.78 mL, 14.5 mmol) using a procedure analogous to Step AC (1) to afford 6-chloro-2-(2,4-difluorophenyl)hexanoic acid (3.39 g, 89% yield). LC-MS (M−H)− 261.1. The crude product was used for subsequent chemistry without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08349880B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-fbd92aeccb2a4086b94935b0136d51b9 |
| Source note | uspto-grants-2013_01 |