Dichloromethane → HCID 66593487, compound

HRID 1917008Notes

Reaction equation

HRID 1917008 reaction equation
C(Cl)Cl.[C:4]([C:8]1[CH:9]=[C:10]([OH:14])[CH:11]=[CH:12][CH:13]=1)([CH3:7])([CH3:6])[CH3:5].[N+:15]([C:18]1[CH:23]=[CH:22][C:21]([O:24][C:25](=O)[O:26]C2C=CC([N+]([O-])=O)=CC=2)=[CH:20][CH:19]=1)([O-:17])=[O:16]>CN(C1C=CN=CC=1)C.CCCCCC.C(OC(=O)C)C>[C:25](=[O:26])([O:24][C:21]1[CH:20]=[CH:19][C:18]([N+:15]([O-:17])=[O:16])=[CH:23][CH:22]=1)[O:14][C:10]1[CH:11]=[CH:12][CH:13]=[C:8]([C:4]([CH3:7])([CH3:5])[CH3:6])[CH:9]=1

Participants

6

Procedure

An oven-dried 25 mL flask was charged with dry CH2Cl2 (5 mL), 3-t-butylphenol (100 mg, 0.67 mmol), bis(4-nitrophenyl)carbonate (405 mg, 1.34 mmol) and 4-DMAP (162 mg, 1.34 mmol). The reaction was stirred overnight at room temperature and then evaporated. Column chromatography (n-hexane/ethylacetate 8:1) yielded 3-t-butylphenyl 4-nitrophenyl carbonate (189 mg, 0.60 mmol, 90%). This carbonate was dissolved in dry CH2Cl2 (8 mL) and 4-DMAP (162 mg, 1.34 mmol) was added. After 15 min, propargylamine (73 mg, 0.085 ml, 1.34 mmol) was added by syringe. The reaction was allowed to stir overnight at room temperature and then evaporated. Column chromatography (n-hexane/ethylacetate 15:1) yielded N-propargyl-3-t-butylphenyl carbamate (93 mg, 0.40 mmol, 60%). 1H NMR (CDCl3, 400 MHz) δ 1.32 (t, 9H), 2.30 (s, 1H), 4.08 (d, J=5.2 Hz, 2H), 5.27 (broad, 1H), 6.97 (d, J=7.2 Hz, 1H), 7.13 (d, J=2.0 Hz, 1H), 7.23-7.31 (m, 2H); 13C NMR (CDCl3, 100 MHz) δ 30.9, 31.2, 34.7, 72.0, 79.3, 118.5, 122.5, 128.8, 150.6, 152.9, 154.2.

Workup

  1. customevaporated

Sources & evidence

ORD record
ord-7034cf501ac7473a93b3c14075d5012a
Source dataset
uspto-grants-2013_12
Patent number
US08618162B2

Reaction notes

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