Hydrochloric Acid → (+-)-trans-4-Methylene-2-phenylcyclopentanecarboxaldehyde

Temperature

-70 °C

To a solution of oxalyl chloride (1.16 mL, 13.3 mmol) in methylene chloride (50 mL) at −70° C. was added dropwise DMSO (1.88 mL, 26.6 mmol). After 15 min, a solution of (+−)-trans-1-hydroxymethyl-4-methylene-2-phenylcyclopentane from Step B (1.0 g, 5.3 mmol) in methylene chloride (10 mL) was added. The reaction was stirred at −70° C. for 1.5 h and then DIPEA (9.25 mL, 53 mmol) in methylene chloride (10 mL) was added dropwise over 5 min. After a further 10 min, the mixture was allowed to warm to rt for 1 h and then diluted with methylene chloride and poured into dilute aq. HCl. The layers were separated. The aq. layer was reextracted with a second portion of methylene chloride and the organic layers were each washed with brine, dried over sodium sulfate, combined and concentrated in vacuo. The residue was purified by FC (20% ethyl acetate in hexanes) to give the title product (0.88 g) after vacuum drying.

1. waitAfter a further 10 min
2. temperatureto warm to rt for 1 h
3. customThe layers were separated
4. washeach washed with brine
5. dry with materialdried over sodium sulfate
6. concentrationconcentrated in vacuo
7. customThe residue was purified by FC (20% ethyl acetate in hexanes)

ORD record

ord-01202aaa687940039d0fb039db1e3e04

Source dataset

uspto-grants-2002_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06472410B1