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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917008Generated: November 1, 2026

Dichloromethane → HCID 66593487, compound

https://huagongshe.com/reaction/1917008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPhenol, 3-(1,1-dimethylethyl)-HCID 11450—
ReactantBis(4-nitrophenyl) carbonateHCID 78756—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 66593487HCID 6659348790%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618162B2
Source datasetuspto-grants-2013_12
ORD IDord-7034cf501ac7473a93b3c14075d5012a
Source noteuspto-grants-2013_12