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Tetrahydrofuran → 3-(5-Fluorobenzothiazol-2-ylmethoxy)benzyl bromide

HRID 1200610
Notes
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Reaction equation

HRID 1200610 reaction equation
[C:21]([Br:22])([Br:23])([Br:24])[Br:25].[F:1][c:2]1[cH:3][cH:4][c:5]2[c:6]([n:7][c:8]([CH2:10][O:11][c:12]3[cH:13][c:14]([CH2:15][OH:16])[cH:17][cH:18][cH:19]3)[s:9]2)[cH:20]1.[O:45]1[CH2:46][CH2:47][CH2:48][CH2:49]1.[c:26]1([P:27]([c:28]2[cH:29][cH:30][cH:31][cH:32][cH:33]2)[c:34]2[cH:35][cH:36][cH:37][cH:38][cH:39]2)[cH:40][cH:41][cH:42][cH:43][cH:44]1>>[F:1][c:2]1[cH:3][cH:4][c:5]2[c:6]([n:7][c:8]([CH2:10][O:11][c:12]3[cH:13][c:14]([CH2:15][Br:22])[cH:17][cH:18][cH:19]3)[s:9]2)[cH:20]1
ParticipantsSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 8028TetrahydrofuranHCID 11205Carbon tetrabromideHCID 11776TriphenylphosphineHCID 536375833-(5-Fluorobenzothiazol-2-ylmethoxy)benzyl alcohol

Product 1

HCID 190194713-(5-Fluorobenzothiazol-2-ylmethoxy)benzyl bromide

Sources & evidence

ORD record
ord-53847b8e988841f0b3ebc2ae4c543138
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (5/10)
On this pageParticipantsSources & evidenceReaction notes
DOI
10.1039/C8SC04228D

Reaction notes

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