HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → trans-Racemic-2-(4-iodophenyl)cyclohexyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | trans-Racemic-2-phenylcyclohexyl acetate | HCID 11009435 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | trans-Racemic-2-(4-iodophenyl)cyclohexyl acetate | HCID 90041487 | — |
Reaction Steps
To a stirred solution of trans-racemic-2-phenylcyclohexyl acetate (5.60 g, 25.7 mmol) under nitrogen in TFA (50 ml) at 0° C. was added N-iodosuccinimide (5.77 g, 25.7 mmol) portionwise over 5 minutes. The mixture was allowed to warm and stir at room temperature for 3 hours. The mixture was concentrated under reduced pressure. The resultant oil was chromatographed using an 80 g silica gel cartridge eluted with 0-20% ethyl acetate in hexanes over 15 column volumes. The desired product fractions were combined and concentrated under reduced pressure to provide the desired product as a yellow oil. LC-MS: calculated for C14H17IO2 344.19 observed m/e: 345.33 (M+H)+ (Rt 2.60/4 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09290517B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-d17b8046538c4ca4af1701e6dbd5ac80 |
| Source note | uspto-grants-2016_03 |