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4-Hydroxybenzaldehyde → 1-(4-(Azetidin-3-yloxy)benzyl)azetidine

HRID 1035206
Notes
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Reaction equation

HRID 1035206 reaction equation
[CH3:1][N:2]([CH2:4][C:5]1[CH:22]=[CH:21][C:8]([O:9][CH:10]2[CH2:13][N:12](C(OC(C)(C)C)=O)[CH2:11]2)=[CH:7][C:6]=1C)[CH3:3].N1CC(OC2C=CC(CN(C)C)=C(C)C=2)[CH2:25]1.N1CCC1.OC1C=CC(C=O)=CC=1>>[NH:12]1[CH2:13][CH:10]([O:9][C:8]2[CH:21]=[CH:22][C:5]([CH2:4][N:2]3[CH2:3][CH2:25][CH2:1]3)=[CH:6][CH:7]=2)[CH2:11]1
ParticipantsProcedureSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 1264-HydroxybenzaldehydeHCID 10422AzetidineHCID 58043102tert-Butyl 3-(4-((dimethylamino)methyl)-3-methylphenoxy)azetidine-1-carboxylateHCID 666563501-(4-(Azetidin-3-yloxy)-2-methylphenyl)-N,N-dimethylmethanamine

Product 1

HCID 666534951-(4-(Azetidin-3-yloxy)benzyl)azetidineYield 39%

Procedure

On this pageParticipantsProcedureSources & evidenceReaction notes

Using similar protocols as described in Examples 20A, 20B and 20C employing azetidine and 4-hydroxybenzaldehyde as starting material afforded 0.44 g (39%) of 41A as an oil. 1H NMR (500 MHz, CDCl3): δ 2.06 (m, 2H), 3.18 (m, 4H), 3.35 (t, 1H), 3.48 (s, 2H), 3.66 (t, 1H), 3.8-5.0 (m, 3H), 6.71 (m, 2H), 7.16 (d, 2H).

Sources & evidence

ORD record
ord-48605add3136462ebe946ee8f998c2a6
Source dataset
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08546375B2

Reaction notes

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