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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434175Generated: October 30, 2026

Tributylstannane → HCID 12151499, compound

https://huagongshe.com/reaction/434175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylstannaneHCID 5948—
ReactantAzobisisobutyronitrileHCID 6547—
ReactantIndolineHCID 10328—
SolventBenzeneHCID 241—
ProductHCID 12151499HCID 12151499—

Reaction Steps

A three-hour addition of nBu3SnH (154 μL, 573 μmol) and AIBN (34 mg, 208 μmol) solution in benzene (1 mL) to a refluxing solution of the unpurified ketimine (125 mg, 521 μmol) in benzene (50 mL) delivered, after flash chromatography (30% CH2Cl2 Hexanes) 0.024 g (30%) of the desired indoline as a colorless oil. Rf=0.1 (30% CH2Cl2 Hexanes); IR (film) 3047, 1607 cm−1; 1H NMR (400 MHz, CDCl3) δ 7.04 (t, J=6.7 Hz, 2H), 6.59 (t, J=7.4 Hz, 1H), 6.42 (d, J=8.1 Hz, IH), 3.83 (sep, J=6.6 Hz, 1H), 3.33 (t, J=8.5 Hz, 2H), 2.93 (t, J=8.3 Hz, 2H), 1.15 (d, J=6.7 Hz, 6H); 13C NMR (100 MHz, CDCl3) ppm 151.5, 130.5, 127.5, 124.6, 117.1, 107.3, 46.0, 45.7, 28.4, 18.4; HRMS (EI) Exact mass calcd for C11H15N [M]+, 161.1204. Found 161.1201.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06670479B2
Source datasetuspto-grants-2003_12
ORD IDord-d731ee8c1259441c8d689cd3412b95b4
Source noteuspto-grants-2003_12