Sodium Iodide → ((R)-1,3,3-Trimethyl-butyl)-carbamic acid tert-butyl ester

To a solution of methanesulfonic acid (S)-2-tert-butoxycarbonylamino-4,4-dimethyl-pentyl ester (250 mg, 0.380 mmol) under nitrogen atmosphere in DME (4 mL) were added successively sodium iodide (569 mg, 3.80 mmol) and zinc powder (248 mg, 3.80 mmol). The dark mixture was stirred at RT overnight. After completion of the reaction a saturated aqueous solution of NH4Cl (3 mL) was slowly added, followed by CH2Cl2 (3 mL) and the resulting biphasic mixture was stirred at RT for 30 min. Few crystals of Na2S were added and the mixture was further stirred for 1 h. The mixture was filtered through a pad of celite, the organic layer was separated, washed with brine, dried (Na2SO4), filtered and concentrated. The crude mixture was purified by flash chromatography on silica gel (c-hexane to c-hexane/EtOAc 8:2) the desired material as a white powder. TLC, Rf (c-hexane/EtOAc 1:1): 0.50; 1H NMR (400 MHz, DMSO-d6) δ (ppm): 6.60 (d, 1H), 3.61 (m, 1H), 1.42 (dd, 1H), 1.38 (s, 9H), 1.15 (dd, 1H), 1.00 (d, 3H), 0.88 (s, 9H).

1. additionwas slowly added
2. stirringthe resulting biphasic mixture was stirred at RT for 30 min
3. additionFew crystals of Na2S were added
4. stirringthe mixture was further stirred for 1 h
5. filtrationThe mixture was filtered through a pad of celite
6. customthe organic layer was separated
7. washwashed with brine
8. dry with materialdried (Na2SO4)
9. filtrationfiltered
10. concentrationconcentrated
11. customThe crude mixture was purified by flash chromatography on silica gel (c-hexane to c-hexane/EtOAc 8:2) the desired material as a white powder

ORDレコード

ord-911ee997be084e2b8dbf300ea2904395

出典データセット

uspto-grants-2016_07

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US09388199B2