돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1888683생성일: 2026년 10월 27일

Triethylamine → HCID 178441311, 화합물

https://huagongshe.com/reaction/1888683

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1,2,2-Trimethyl-1,3-cyclopentanedicarboxylic acidHCID 21491—
반응물Phosphorus pentachlorideHCID 24819—
반응물2-tert-Butyl-4-butylisothiazol-5(2H)-imineHCID 66867228—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
용매Ethyl AcetateHCID 8857—
생성물HCID 178441311HCID 17844131142%

반응 단계

A mixture of (+)-camphoric acid (Aldrich, 2.00 g, 10.0 mmol) and phosphorus pentachloride (Aldrich, 4.16 g, 20.0 mmol) in hexane (75 mL) was heated to reflux and stirred for 24 hours. After cooling to ambient temperature, the reaction mixture was concentrated by rotary evaporator to give a pale yellow oil. The crude bis acid chloride (474 mg, 2.00 mmol) was added to a mixture of the product from Example 92B (425 mg, 2.00 mmol) and triethylamine (1.01 g, 10.0 mmol) in anhydrous tetrahydrofuran (12 mL). The mixture was stirred for 2 hours Anhydrous methanol (10 mL) was added and the resulting mixture was stirred overnight. The mixture was concentrated by rotary evaporator to give a brown oil. Flash chromatography (silica gel, 5-25% ethylacetate in hexanes) afforded 343 mg (42%) of the title compound. 1H NMR (DMSO-d6) δ 0.53 (s, 3H), 0.90 (t, J=7.3 Hz, 3H), 1.20 (s, 3H), 1.23 (s, 3H), 1.23-1.40 (m, 2H), 1.41-1.50 (m, 1H), 1.57 (s, 9H), 1.57-1.67 (m, 2H), 1.71-1.84 (m, 1H), 2.24-2.36 (m, 1H), 2.41-2.48 (m, 1H), 2.61-2.67 (m, 2H), 3.00-3.06 (m, 1H), 3.59 (s, 3H), 8.52 (s, 1H). MS (ESI+) m/z 409 (M+H)+. Anal. calcd. for C22H36N2O3S: C, 64.67; H, 8.88; N, 6.86. Found: C, 64.52; H, 8.76; N, 6.84.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08501794B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-ccf2d8a587934c3fb2a03827fc1a39bc
출처 메모uspto-grants-2013_08